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4 In 1 Cutting Block Template ''Wright M
FDA UDIClass II (US FDA UDI)
by Brainlab SE
Identity
- Trade Name
- 4 In 1 Cutting Block Template ''Wright M FDA UDI
- Generic Name
- Robotic surgical navigation system FDA UDI
- Model / Reference
- 52465 FDA UDI
Identifiers
- Catalog Number
- 52465 FDA UDI
- Primary DI / UDI-DI
- 04056481005900 FDA UDI
- 510(k) Number
- K102990 FDA UDI
- FDA Product Code
- OLO FDA UDI
- GMDN Term
- Robotic surgical navigation system 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
No
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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
4 In 1 Cutting Block Template ''Wright M by Brainlab SE — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K102990 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
- Brainlab SE
Sources (1)
- FDA UDI 60529610-191c-4366-9b0b-3c63ea2d5b7f 36 fields · synced May 31, 2026