← Back to catalogue
Retractor, Wound, acc. Henly side-Blade 50mm for 30-0720 (pair)
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- Retractor, Wound, acc. Henly side-Blade 50mm for 30-0720 (pair) FDA UDI
- Generic Name
- Self-retaining surgical retractor, reusable FDA UDI
- Device Name
- Retractor, Wound, acc. Henly side-Blade 50mm for 30-0720 (pair) FDA UDI
- Model / Reference
- 30-0720.50 FDA UDI
- Description
- Retractor, Wound, acc. Henly side-Blade 50mm for 30-0720 (pair) FDA UDI
Identifiers
- Catalog Number
- 30-0720.50 FDA UDI
- Primary DI / UDI-DI
- 04057034110089 FDA UDI
- FDA Product Code
- DWS FDA UDI
- GMDN Term
- Self-retaining surgical retractor, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 870.4500 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Self-retaining surgical retractor, reusable
Retractor, Wound, acc. Henly side-Blade 50mm for 30-0720 (pair) by Geister Medizin Technik GmbH — Class I — FDA UDI — listed in FDA GUDID
Similar devices
Also classified as Self-retaining surgical retractor, reusable.
- Avalign — AVALIGN TECHNOLOGIES, Inc. · Class I
- Avalign — AVALIGN TECHNOLOGIES, Inc. · Class II
- Millennium — AVALIGN TECHNOLOGIES, Inc. · Class II
- Surgical Direct — SURGICAL DIRECT, INC. · Class I
- Symmetry Cloward — SYMMETRY SURGICAL INC. · Class II
- Life Instruments — Life Instrument Corporation · Class I
- Integra® Miltex® — Integra LifeSciences Production Corporation · Class I
- SELF RETAINING CORONOID RETRACTOR CHAIN WITH RINGS — W.H. Holden, Inc. · Class I
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Geister Medizin Technik GmbH
Sources (1)
- FDA UDI cf102543-5f1b-4536-86d4-7133e3a47813 35 fields · synced May 30, 2026