Identity
- Trade Name
- CARROLL TENDON PULLING FORCEPS FDA UDI
- Generic Name
- Nerve/vessel retractor FDA UDI
- Device Name
- CARROLL TENDON PULLING FORCEPS SERRATED TIP CURVED DOWN SHAFT QUANTUM FDA UDI
- Model / Reference
- 350-805Q FDA UDI
- Description
- CARROLL TENDON PULLING FORCEPS SERRATED TIP CURVED DOWN SHAFT QUANTUM FDA UDI
Identifiers
- Catalog Number
- 350-805Q FDA UDI
- Primary DI / UDI-DI
- 00192896093614 FDA UDI
- FDA Product Code
- HTZ FDA UDI
- GMDN Term
- Nerve/vessel retractor FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 5 Inch FDA UDI
Category: Nerve/vessel retractor
A comprehensive medical device directory entry for the CARROLL TENDON PULLING FORCEPS, a hand-held instrument used in orthopedic surgery to retract nerves, tendons, or blood vessels.
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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
- Sontec Instruments, Inc.
Sources (1)
- FDA UDI bc4090a9-0283-49d7-a751-19dc619adf38 36 fields · synced Jun 27, 2026