← Back to catalogue
Self-retaining retractor acc. to Weitlan 2x3 prongs sharp L=110mm
FDA UDIEUDAMEDClass II (US FDA UDI)
Identity
- Trade Name
- Self-retaining retractor acc. to Weitlan 2x3 prongs sharp L=110mm FDA UDI
- Generic Name
- Surgical retraction system mounting frame, reusable FDA UDI
- Device Name
- Self-retaining retractor acc. to Weitlan 2x3 prongs sharp L=110mm FDA UDI
- Model / Reference
- UL7050-11 FDA UDI
- Description
- Self-retaining retractor acc. to Weitlan 2x3 prongs sharp L=110mm FDA UDI
Identifiers
- Catalog Number
- UL7050-11 FDA UDI
- Primary DI / UDI-DI
- 04057034261521 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
Self-retaining retractor acc. to Weitlan 2x3 prongs sharp L=110mm by Geister Medizin Technik GmbH — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED
Similar devices
Also classified as Surgical retraction system mounting frame, reusable.
- Novo Surgical — NOVO SURGICAL, INC. · Class I
- gSource — GSOURCE, LLC. · Class I
- Hayden Medical — Hayden Medical Inc · Class I
- Millennium — AVALIGN TECHNOLOGIES, Inc. · Class II
- V. Mueller — STERIS CORPORATION · Class I
- Hayden Medical — Hayden Medical Inc · Class I
- Novo Surgical — NOVO SURGICAL, INC. · Class I
- Millennium — AVALIGN TECHNOLOGIES, Inc. · Class II
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class II | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Geister Medizin Technik GmbH
Sources (2)
- FDA UDI c5500159-de7a-4831-bdbb-2753a8683e41 35 fields · synced Jun 18, 2026
- EUDAMED 1 fields · synced Jun 4, 2026