Identity
- Trade Name
- Cook Bx FDA UDI
- Generic Name
- Needle guide, reusable FDA UDI
- Device Name
- Cook, Bx Core Tissue Biopsy Device FDA UDI
- Model / Reference
- G46045 FDA UDI
- Description
- Cook, Bx Core Tissue Biopsy Device FDA UDI
Identifiers
- Catalog Number
- CBX-1 FDA UDI
- Primary DI / UDI-DI
- 00827002460454 FDA UDI
- FDA Product Code
- KNW FDA UDI
- GMDN Term
- Needle guide, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1075 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
Category: Needle guide, reusable
Cook Bx by Cook Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 II | Pending data |
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Manufacturer
- Manufacturer
- Cook Incorporated
Sources (1)
- FDA UDI c121c934-eb3d-43be-acc3-3b9045cf5057 36 fields · synced Jun 8, 2026