Aesculap DO303R
by Aesculap AG
Ref DO303R
Aesculap DO303R is a Class I device made by Aesculap AG, registered in EUDAMED on 16 Sep 2025 (Basic UDI-DI 40392390000018012G) and listed in FDA GUDID since 17 Jun 2020 (UDI-DI 04038653037179), active as of 12 Nov 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number40392390000018012G 04038653037179 | Date16 Sep 2025 | StatusActive |
| United States | GUDID listing GUDID | Number04038653037179 | Date17 Jun 2020 | StatusListed |
Official records
- EUDAMED public site 40392390000018012G
- AccessGUDID record 04038653037179
Across registries
- EUDAMED Basic UDI-DI 40392390000018012G registered 16 Sep 2025 Active
- FDA GUDID UDI-DI 04038653037179 listed 17 Jun 2020 Listed
Timeline
- Listed FDA GUDID 04038653037179
- Registered EUDAMED 40392390000018012G
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Aesculap
- Generic name
- Gauze packer
- Device name
- Tampon/thread tamper
- Model / Ref / Catalog
- DO303R
- Primary DI / UDI-DI
- 04038653037179
- Basic UDI-DI
- 40392390000018012G
- FDA product code
- DZN
- EMDN code
- L159003 Dental and periodontal probes and explorers, reusable
- GMDN term
- Gauze packer
- Device class
- Class I
- Regulation number
- 872.4565
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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