Identity
- Trade Name
- WECK FDA UDI
- Generic Name
- Skin stapler/staple, non-bioabsorbable FDA UDI
- Device Name
- VISISTAT 35W NON-STERILE FDA UDI
- Model / Reference
- IPN914814 FDA UDI
- Description
- VISISTAT 35W NON-STERILE FDA UDI
Identifiers
- Catalog Number
- 528236 FDA UDI
- Primary DI / UDI-DI
- 14026704672896 FDA UDI
- FDA Product Code
- GDT FDA UDI
- GMDN Term
- Skin stapler/staple, non-bioabsorbable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4760 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Ethylene Oxide FDA UDI
Dimensions & Sizes
- Size
- Length — 6.5 Inch FDA UDI
Category: Skin stapler/staple, non-bioabsorbable
Weck by Teleflex Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Skin stapler/staple, non-bioabsorbable.
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- TSRH® Spinal System — MEDTRONIC SOFAMOR DANEK, INC. · Class II
- Multifire Premium — Covidien LP · Class I
- REFLEX — Conmed Corporation · Class I
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Teleflex Incorporated
Sources (1)
- FDA UDI 6704875a-0d2e-4613-bd21-8a3e8d5b3b4e 36 fields · synced May 31, 2026