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Arterial Hemostatic Device
Siri Peranti Perubatan Kelas II

Arterial Hemostatic Device

Suitable for closed compression hemostasis at puncture site, insertion site, or catheter wound site after arterial interventional procedures.

Suitable for closed compression hemostasis at puncture site, insertion site, or catheter wound site after arterial interventional procedures. The arteriovenous hemostatic device consists of five parts: fixation strap, compression plate, elastic pad, hemostatic sponge, and release paper. According to different fixation methods, it is divided into standard type and reinforced type. The reinforced type adds an independent fixation strap on the basis of the standard type. The fixation strap is made of medical elastic adhesive tape, the compression plate is formed from medical polypropylene, the elastic pad is a medical soft polyurethane foam pad connected to a hemostatic sponge, and the hemostatic sponge is made of Chitosan. The product is sterilized by irradiation, provided in sterile state, and for single use.

Kuantiti Pesanan Minimum (MOQ)

—

Tempoh Sampel

7–14 hari

Masa Penghantaran Pengeluaran

25–35 hari

Mod Perkhidmatan

OEM · ODM · Label Peribadi (Private Label)

Specifications / Attributes

  • Class II Medical Device Registration Certificate (Hunan Medical Device Registration)
  • Main components: fixation strap, compression plate, elastic pad, hemostatic sponge, release paper (five parts)
  • Sterile Supply (Irradiation Sterilization)
  • Supports OEM / ODM Custom Development of specifications and packaging

Technical Specifications

  • Registration Certificate No.: Hunan Medical Device Registration 20242141212
  • Model: Arteriovenous Hemostatic Device
  • Sterility: Sterile Supply

Why Weitai

Mengapa pilih Weitai?

Kosmetik × Peranti Perubatan dwi kelayakan, dari formulasi hingga pengeluaran besar-besaran boleh dikawal sepenuhnya.

Weitai
Typical OEM Factory
Sistem Kelayakan
Kosmetik + Peranti Perubatan Kelas II/III dwi kelayakan (ISO 13485 / ISO 22716 / GMPC)
Hanya kelayakan kosmetik tunggal
Bengkel Bersih
Bengkel bersih GMP kelas 100,000/10,000, meliputi barisan pengeluaran lyophilized, pengisian, gel dan pembalut
Bengkel penulenan biasa
Sokongan Sijil Pendaftaran
110+ sijil pendaftaran peranti perubatan + sokongan penuh proses pendaftaran kosmetik
Hanya OEM, tiada sokongan sijil pendaftaran
Kekuatan R&D
72 paten ciptaan, 30+ paten antarabangsa, sokongan data klinikal
Terutamanya penyalinan pustaka formulasi
Keupayaan Sampel
Sampel tersuai 7–14 hari, formulasi dirahsiakan sepenuhnya
Terutamanya produk standard, tempoh tersuai panjang
Liputan Kategori
Rantaian penuh kosmetik / peranti perubatan / pengisi suntikan Kelas III
Terutamanya kategori tunggal

Process

Proses Kerjasama

Enam langkah piawai, dari idea hingga pasaran boleh dikawal sepenuhnya.

01

Komunikasi Keperluan

Jelaskan jenis produk, spesifikasi, kuantiti, pasaran sasaran dan keperluan pematuhan.

02

Formulasi dan Sampel

Pasukan R&D menyesuaikan formulasi, menyediakan sampel untuk penilaian dan pengubahsuaian.

03

Pengesahan dan Sebut Harga

Sahkan formulasi, pembungkusan dan MOQ, tandatangani perjanjian kerjasama.

04

Pengeluaran Massa dan Kawalan Kualiti

Organisasi pengeluaran mengikut piawaian GMP, pemantauan kualiti sepanjang proses.

05

Pembungkusan dan Label Jenama

Selesaikan pengisian, pembungkusan dan pelabelan mengikut kehendak pihak jenama.

06

Penghantaran dan Pelepasan

Pemeriksaan penghantaran, sediakan dokumen pematuhan, uruskan penghantaran logistik.

Packaging

Pilihan Pembungkusan

Menyokong pelbagai bentuk pembungkusan dan penyesuaian jenama.

Botol

Bottle

Tiub

Tube

Balang

Jar

Ampul

Ampoule

Dwi Kebuk Lyophilized

Lyophilized Dual-Chamber

Pek Topeng Muka

Mask Sachet

FAQ

Soalan Lazim

Mengenai OEM, sampel dan pematuhan, mungkin anda ingin tahu.

What is your minimum order quantity (MOQ)?+

MOQ varies by product. Medical gels and dressings generally start from 10,000 units, while skin care can be lower. It depends on the product and formula—please contact us for a quote.

What certifications does Weitai Group hold?+

Weitai Group is fully qualified: certified with ISO13485 (medical device quality management) and ISO22716/GMPC (cosmetics GMP), recognized as a National High-Tech Enterprise, and certified with GB/T29490 IP management system. We hold 110+ Class II medical device registrations, 72 invention patents and 30+ international patents, operate 100,000-class GMP cleanrooms across six production bases totaling 150,000 m² with 65 automated production lines, and bring 25+ years of OEM/ODM experience serving 1000+ partner brands.

What is the difference between ODM and OEM?+

OEM manufactures your existing formulas and machines under your brand; ODM offers full customization from formula development, packaging design to registration. Weitai supports both and provides free formula development and documentation kits.

Can you provide formula development?+

Yes. With a 105-person R&D team, Weitai offers free formula development, packaging design, and documentation kits (brochures, detail pages, test reports) plus assistance with registration.

How can I get a quote?+

Please submit your product requirements and quantities via the inquiry form or sales@zhenmeifu.com. Our dedicated sales will contact you within 24 hours with a proposal and quotation.

Bolehkah melakukan OEM untuk pengisi suntikan mikrosfera PLLA (asid poli-L-laktik)?+

Boleh. Weitai menyokong OEM/ODM untuk produk pengisi suntikan Kelas III Medical Device, termasuk pengisi suntikan mikrosfera PLLA (asid poli-L-laktik). Saiz mikrosfera seragam dan boleh dikawal, biodegradasi, formula boleh disesuaikan dan Aseptic Filling.

Serahkan idea produk anda kepada rakan yang boleh dipercayai

Bring your product idea to a reliable partner — from formula and sample to mass production, Weitai walks with you end to end.