Identity
- Trade Name
- Retractor, Spinal, Speculum longitudinal FDA UDI
- Generic Name
- Surgical retraction system mounting frame, reusable FDA UDI
- Device Name
- Retractor, Spinal, Speculum longitudinal SpineControl™ FDA UDI
- Model / Reference
- 29-3011 FDA UDI
- Description
- Retractor, Spinal, Speculum longitudinal SpineControl™ FDA UDI
Identifiers
- Catalog Number
- 29-3011 FDA UDI
- Primary DI / UDI-DI
- 04057034097069 FDA UDI
- FDA Product Code
- GZT FDA UDI
- GMDN Term
- Surgical retraction system mounting frame, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4800 FDA UDI
- Commercial Distribution
- 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Surgical retraction system mounting frame, reusable
Retractor, Spinal, Speculum longitudinal by Geister Medizin Technik GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Surgical retraction system mounting frame, reusable.
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- Millennium — AVALIGN TECHNOLOGIES, Inc. · Class II
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 II | Pending data |
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Manufacturer
- Manufacturer
- Geister Medizin Technik GmbH
Sources (1)
- FDA UDI 7a279ba5-97ed-497b-8b4a-1daf859d5c09 35 fields · synced May 29, 2026