Identity
- Trade Name
- TRIO FDA UDI
- Generic Name
- Surgical instrument guard, reusable FDA UDI
- Device Name
- TISSUE PROTECTION SLEEVE FOR TAP FDA UDI
- Model / Reference
- 48905010 FDA UDI
- Description
- TISSUE PROTECTION SLEEVE FOR TAP FDA UDI
Identifiers
- Catalog Number
- 48905010 FDA UDI
- Primary DI / UDI-DI
- 07613327273113 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Surgical instrument guard, 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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Trio by Stryker Corp. — 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
- Stryker Corp.
Sources (1)
- FDA UDI d40737db-ae0f-408a-9a81-7f6a3fe405b3 35 fields · synced Jun 8, 2026