Identity
- Trade Name
- MOSS FDA UDI
- Generic Name
- Bone tap, reusable FDA UDI
- Device Name
- MOSS MIAMI MAGNUM SPINE SYSTEM TAP SHAFT 6.35 5mm 30-60mm Plus or Minus 1.00 Percent FDA UDI
- Model / Reference
- 275010350 FDA UDI
- Description
- MOSS MIAMI MAGNUM SPINE SYSTEM TAP SHAFT 6.35 5mm 30-60mm Plus or Minus 1.00 Percent FDA UDI
Identifiers
- Catalog Number
- 275010350 FDA UDI
- Primary DI / UDI-DI
- 10705034194103 FDA UDI
- FDA Product Code
- HWX FDA UDI
- GMDN Term
- Bone tap, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 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 11087a4f-938a-40e7-b2e0-1100359d09ff 36 fields · synced May 31, 2026