Identity
- Trade Name
- WECK FDA UDI
- Generic Name
- Scalp wound clip FDA UDI
- Device Name
- RANEY CLIPS DISPOSABLE FDA UDI
- Model / Reference
- IPN009317 FDA UDI
- Description
- RANEY CLIPS DISPOSABLE FDA UDI
Identifiers
- Catalog Number
- 658505 FDA UDI
- Primary DI / UDI-DI
- 04026704418343 FDA UDI
- FDA Product Code
- HBO FDA UDI
- GMDN Term
- Scalp wound clip FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4150 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 0.625 Inch FDA UDI
Category: Scalp wound clip
Weck by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Scalp wound clip.
- Gimmi — Gimmi GmbH · Class I
- Clip Gun — Medtronic PS Medical · Class II
- Gimmi — Gimmi GmbH · Class I
- Sklar — Sklar Corporation · Class I
- RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
- Sklar — Sklar Corporation · Class I
- Gimmi — Gimmi GmbH · Class I
- Sklar — Sklar Corporation · Class I
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 II | Pending data |
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Manufacturer
- Manufacturer
- Teleflex Incorporated
Sources (1)
- FDA UDI 4db4a635-7930-4a33-9aa0-b90e733fa4cf 36 fields · synced Jun 6, 2026