Tonsil dissecting forceps 40-406-20
by Spiggle & Theis Medizintechnik GmbH
Ref 40-406-20
Tonsil dissecting forceps 40-406-20 is a Class I device made by Spiggle & Theis Medizintechnik GmbH, registered in EUDAMED on 30 Sep 2026 (Basic UDI-DI B-04250381888056) and listed in FDA GUDID since 26 Sep 2022 (UDI-DI 04250381888056), active as of 25 Oct 2026.
Active
CE MDD
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/MDD EUDAMED | NumberB-04250381888056 04250381888056 | Date30 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04250381888056 | Date26 Sep 2022 | StatusListed |
Official records
- EUDAMED public site B-04250381888056
- AccessGUDID record 04250381888056
Across registries
- EUDAMED Basic UDI-DI B-04250381888056 registered 30 Sep 2026 Active
- FDA GUDID UDI-DI 04250381888056 listed 26 Sep 2022 Listed
Timeline
- Listed FDA GUDID 04250381888056
- Registered EUDAMED B-04250381888056
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Tonsil dissecting forceps
- Generic name
- Surgical soft-tissue manipulation forceps, tweezers-like, reusable
- Device name
- Forceps (Tweezers)
- Model / Ref / Catalog
- 40-406-20
- Description
- 1:2 teeth, large 2.5 mm, 20.5 cm
- Primary DI / UDI-DI
- 04250381888056
- Basic UDI-DI
- B-04250381888056
- FDA product code
- LRC
- EMDN code
- L031308 Surgical and anatomical tweezers, reusable
- GMDN term
- Surgical soft-tissue manipulation forceps, tweezers-like, reusable
- Device class
- Class I
- Regulation number
- 874.4420
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices in this category
Other devices filed under SURGICAL AND ANATOMICAL TWEEZERS, REUSABLE.