Identity
- Trade Name
- PlusDrive FDA UDI
- Generic Name
- Surgical screwdriver, reusable FDA UDI
- Device Name
- 2.0MM PLUSDRIVE(TM) EXTRA LNG SCREWDRIVER W/HOLDING SLEEVE FDA UDI
- Model / Reference
- SD313.251 FDA UDI
- Description
- 2.0MM PLUSDRIVE(TM) EXTRA LNG SCREWDRIVER W/HOLDING SLEEVE FDA UDI
Identifiers
- Catalog Number
- SD313251 FDA UDI
- Primary DI / UDI-DI
- 10887587002194 FDA UDI
- FDA Product Code
- HXX FDA UDI
- GMDN Term
- Surgical screwdriver, 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
PlusDrive 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 97209a1c-07d6-46f2-9656-7174dbfa3258 36 fields · synced May 30, 2026