Identity
- Trade Name
- Mazor X Scan & Plan Disposable Kit FDA UDI
- Generic Name
- Orthopaedic surgical procedure kit, non-medicated, single-use FDA UDI
- Device Name
- Mazor X Scan & Plan Disposable Kit FDA UDI
- Model / Reference
- KIT0571-03 FDA UDI
- Description
- Mazor X Scan & Plan Disposable Kit FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07290109181103 FDA UDI
- FDA Product Code
- OLO FDA UDIHAW FDA UDILLZ FDA UDI
- GMDN Term
- Orthopaedic surgical procedure kit, non-medicated, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4560 FDA UDI892.2050 FDA UDI
- Commercial Distribution
- Not 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
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Mazor X Scan & Plan Disposable Kit by Mazor Robotics Ltd — 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
- Mazor Robotics Ltd
Sources (1)
- FDA UDI 7b800972-6e00-40b7-a0ba-1d8e107b3c15 35 fields · synced Jun 8, 2026