Identity
- Trade Name
- Symmetry Surgical FDA UDI
- Generic Name
- Surgical retractor/retraction system blade, reusable FDA UDI
- Device Name
- BLADE RETRACTOR 1IN X 3 1/3IN MEDIUM TITANIUM ULTRA BOOKLER MEYERDING ULTRA INSTRUMENTS FDA UDI
- Model / Reference
- 58-0071T FDA UDI
- Description
- BLADE RETRACTOR 1IN X 3 1/3IN MEDIUM TITANIUM ULTRA BOOKLER MEYERDING ULTRA INSTRUMENTS FDA UDI
Identifiers
- Catalog Number
- 58-0071T FDA UDI
- Primary DI / UDI-DI
- 00887482101346 FDA UDI
- FDA Product Code
- GAD FDA UDI
- GMDN Term
- Surgical retractor/retraction system blade, 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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Symmetry Surgical by Symmetry Surgical 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
- Symmetry Surgical Inc.
Sources (1)
- FDA UDI 69461f0d-d055-451a-b3f6-118422f5aa97 35 fields · synced Jun 8, 2026