Identity
- Trade Name
- MOSS FDA UDI
- Generic Name
- Instrument tray, reusable FDA UDI
- Device Name
- MOSS MIAMI SPINE SYSTEM REDUCTION SCREW CADDIE 7mm, 30-55mm FDA UDI
- Model / Reference
- 279772701 FDA UDI
- Description
- MOSS MIAMI SPINE SYSTEM REDUCTION SCREW CADDIE 7mm, 30-55mm FDA UDI
Identifiers
- Catalog Number
- 279772701 FDA UDI
- Primary DI / UDI-DI
- 10705034201177 FDA UDI
- FDA Product Code
- FSM 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
Moss by Depuy 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
- Depuy Spine, Inc.
Sources (1)
- FDA UDI e9e14ec8-bc2c-4cd9-92ba-5a21539dc1e7 36 fields · synced Jun 8, 2026