Ritter frontal sinus bougie 30-121-25
by Spiggle & Theis Medizintechnik GmbH EUDAMEDGUDID
Active
Ref 30-121-25
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD EUDAMED | NumberB-04250381812648 | Date30 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04250381812648 | Date19 Sep 2022 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Recalls
No FDA recalls on record, checked 25 Oct 2026.
Specification
- Trade Name
- Ritter frontal sinus bougie
- Generic Name
- Ear bougie
- Device Name
- Hooks, Needles, Perforators
- Model / Ref / Catalog
- 30-121-25
- Primary DI / UDI-DI
- 04250381812648
- Basic UDI-DI
- B-04250381812648
- FDA Product Code
- LRC
- EMDN Code
- L031102 Exploration probes, reusable
- GMDN Term
- Ear bougie
- Device Class
- Class I
- Regulation Number
- 874.4420
- Market of Registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Other devices from Spiggle & Theis Medizintechnik GmbH
Properties
Other properties (19)
- 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