Identity
- Trade Name
- Baha FDA UDI
- Generic Name
- General external orthopaedic fixation system implantation kit, reusable FDA UDI
- Device Name
- Drill countersink 4mm FDA UDI
- Model / Reference
- 90417 FDA UDI
- Description
- Drill countersink 4mm FDA UDI
Identifiers
- Catalog Number
- 90417 FDA UDI
- Primary DI / UDI-DI
- 09321502012881 FDA UDI
- 510(k) Number
- K100360 FDA UDI
- FDA Product Code
- LXB FDA UDI
- GMDN Term
- General external orthopaedic fixation system implantation kit, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 874.3302 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
No
FDA UDI
Radiation Sterilization FDA UDI
Dimensions & Sizes
- Size
- Length — 4 Millimeter FDA UDI
Category: General external orthopaedic fixation system implantation kit, reusable
Baha by Cochlear Bone Anchored Solutions AB — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K100360 also covers:
- Baha — Cochlear Bone Anchored Solutions AB
- Baha — Cochlear Bone Anchored Solutions AB
- Baha — Cochlear Bone Anchored Solutions AB
- Baha — Cochlear Bone Anchored Solutions AB
- Baha — Cochlear Bone Anchored Solutions AB
- Baha — Cochlear Bone Anchored Solutions AB
- Baha — Cochlear Bone Anchored Solutions AB
- Baha — Cochlear Bone Anchored Solutions AB
- Baha — Cochlear Bone Anchored Solutions AB
- Baha — Cochlear Bone Anchored Solutions AB
- Baha — Cochlear Bone Anchored Solutions AB
- Baha — Cochlear Bone Anchored Solutions AB
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Cochlear Bone Anchored Solutions AB
Sources (1)
- FDA UDI 232dc936-a430-482e-9832-4bcf1321bd6e 37 fields · synced May 30, 2026