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Cirq Robotic Biopsy Drill Bit 3.4 Cranial
FDA UDIClass II (US FDA UDI)
by Brainlab AG
Identity
- Trade Name
- Cirq Robotic Biopsy Drill Bit 3.4 Cranial FDA UDI
- Generic Name
- Surgical instrument assist arm system, power-adjusted FDA UDI
- Model / Reference
- 56405 FDA UDI
Identifiers
- Catalog Number
- 56405 FDA UDI
- Primary DI / UDI-DI
- 04056481141608 FDA UDI
- 510(k) Number
- K210989 FDA UDI
- FDA Product Code
- HAW FDA UDI
- GMDN Term
- Surgical instrument assist arm system, power-adjusted FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4560 FDA UDI
- Commercial Distribution
- Not 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Cirq Robotic Biopsy Drill Bit 3.4 Cranial by Brainlab AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Brainlab AG
Sources (1)
- FDA UDI 19ea2fcc-54c8-44a4-882a-6b830a6fc0dd 35 fields · synced Jun 8, 2026