Identity
- Trade Name
- Perpos Cervical, Cassette Assembly FDA UDI
- Generic Name
- Instrument tray, reusable FDA UDI
- Device Name
- Instruments Tray FDA UDI
- Model / Reference
- 6159-00 FDA UDI
- Description
- Instruments Tray FDA UDI
Identifiers
- Catalog Number
- 6159-00 FDA UDI
- Primary DI / UDI-DI
- 81195401209000 FDA UDI
- FDA Product Code
- OJH FDA UDI
- GMDN Term
- Instrument tray, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Perpos Cervical, Cassette Assembly by Interventional Spine, Inc — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Interventional Spine, Inc
Sources (1)
- FDA UDI 9c3681f1-7476-4d6b-bef8-0972ae8109a1 36 fields · synced May 30, 2026