Identity
- Trade Name
- Sklar FDA UDI
- Generic Name
- Scalp wound clip FDA UDI
- Device Name
- MICHEL CLIP 22MM (1000 UNIT) FDA UDI
- Model / Reference
- 24-1022 FDA UDI
- Description
- MICHEL CLIP 22MM (1000 UNIT) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 30649111319123 FDA UDI
- FDA Product Code
- FZQ FDA UDI
- GMDN Term
- Scalp wound clip FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4320 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
No
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Scalp wound clip
Sklar by Sklar Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Scalp wound clip.
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- Gimmi — Gimmi GmbH · Class I
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- Gimmi — Gimmi GmbH · Class I
- RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
- RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
- WECK — TELEFLEX INCORPORATED · 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
- Sklar Corporation
Sources (1)
- FDA UDI cd16d8f2-d3c2-48e3-b57d-77798d85d1f0 33 fields · synced May 30, 2026