Aesculap
by Aesculap AG EUDAMEDGUDID
Active
Ref FD569R
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number403923900000191734 | Date18 Nov 2025 | StatusActive |
| United States | GUDID listing GUDID | Number04038653160945 | Date10 Aug 2020 | StatusIn distribution |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
- European Union
- United States
Certificates
No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.
Recalls
No FDA recalls on record, checked 22 Oct 2026.
Specification
- Generic Name
- Surgical soft-tissue manipulation forceps, tweezers-like, reusable
- Device Name
- Micro vascular clip applier
- Model / Ref / Catalog
- FD569R
- Primary DI / UDI-DI
- 04038653160945
- Basic UDI-DI
- 403923900000191734
- Direct Marketing DI
- 04038653160945
- FDA Product Code
- HBT
- EMDN Code
- L070801018001 Forceps for the application and removal of vascular clips, reusable
- GMDN Term
- Surgical soft-tissue manipulation forceps, tweezers-like, reusable
- 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
Other properties (20)
- Sterile: No
- Single Use: No
- Implantable: 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