Aesculap
by Aesculap AG Germany EUDAMEDGUDID
Ref OA312R
Product code GADEMDN L170102
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number403923900000119026 | Date15 Sep 2025 | StatusActive |
| United States | GUDID listing GUDID | Number04038653175369 | Date22 Apr 2020 | StatusIn distribution |
Coverage
- Active
- Listed
- Not covered
- European Union
- United States
Specification
- Generic Name
- Nerve/vessel retractor
- Device Name
- Wound and trachea retractor I
- Model / Ref / Catalog
- OA312R
- Primary DI / UDI-DI
- 04038653175369
- Basic UDI-DI
- 403923900000119026
- Direct Marketing DI
- 04038653175369
- FDA Product Code
- GAD
- EMDN Code
- L170102 Ocular and endocular retractors, reusable
- GMDN Term
- Nerve/vessel retractor
- Device Class
- Class I
- Regulation Number
- 878.4800
- Market of Registration
- Germany
- Commercial Distribution
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Manufacturer details
- EUDAMED SRN
- DE-MF-000005504
Other devices from Aesculap AG
Properties & raw data
Show properties, registry sources and raw records
Other properties (21)
- Sterile: No
- Single Use: No
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Serial Number: No
- Expiration Date: No
- Manufacturing Date: No
Sources (2)
- EUDAMED deb0ab44-0bef-4954-be74-dc34bd8f3aeb
- FDA UDI 37cc7dc5-da7c-4e56-9399-d55d23a3b588