Identity
- Trade Name
- BABCOCK FDA UDI
- Generic Name
- Meniscus forceps FDA UDI
- Device Name
- FEA GRSPR 5MM BABCOCK PKG FDA UDI
- Model / Reference
- 7209534 FDA UDI
- Description
- FEA GRSPR 5MM BABCOCK PKG FDA UDI
Identifiers
- Catalog Number
- 7209534 FDA UDI
- Primary DI / UDI-DI
- 03596010475350 FDA UDI
- 510(k) Number
- K970151 FDA UDI
- FDA Product Code
- HET FDA UDI
- GMDN Term
- Meniscus forceps FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.1720 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Meniscus forceps
Babcock by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Meniscus forceps.
- ACUFEX, PITBULL — Smith & Nephew, Inc. · Class I
- PITBULL — Smith & Nephew, Inc. · Class I
- ACUFEX — Smith & Nephew, Inc. · Class I
- ACUFEX, PITBULL — Smith & Nephew, Inc. · Class I
- PITBULL — Smith & Nephew, Inc. · Class I
Cleared under the same submission
K970151 also covers:
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
- Smith & Nephew, Inc.
Sources (1)
- FDA UDI 2d74d86f-5461-4423-83aa-10b592f618b3 36 fields · synced Jun 8, 2026