Identity
- Trade Name
- DCP FDA UDI
- Generic Name
- Surgical instrument/implant rack FDA UDI
- Device Name
- BASIC PLATE SET--DCP® CASE BOTTOM FDA UDI
- Model / Reference
- 305.06 FDA UDI
- Description
- BASIC PLATE SET--DCP® CASE BOTTOM FDA UDI
Identifiers
- Catalog Number
- 30506 FDA UDI
- Primary DI / UDI-DI
- 10886982184450 FDA UDI
- FDA Product Code
- FSM FDA UDI
- GMDN Term
- Surgical instrument/implant rack 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
Dcp by Synthes (u.s.a.) Lp — 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
- Synthes (u.s.a.) Lp
Sources (1)
- FDA UDI 682609d1-f50a-4b02-81a1-c1fcfbd4ff8f 36 fields · synced Jun 8, 2026