Punches
by SPIGGLE & THEIS Medizintechnik GmbH 13 variants
Ref 30-477-20
Punches (30-477-20) is a Class I device made by SPIGGLE & THEIS Medizintechnik GmbH, registered in EUDAMED on 30 Sep 2026 (Basic UDI-DI B-04250676718334) and listed in FDA GUDID since 5 Oct 2025 (UDI-DI 04250676718334), active as of 23 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-04250676718334 04250676718334 | Date30 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04250676718334 | Date5 Oct 2025 | StatusListed |
Official records
- EUDAMED public site B-04250676718334
- AccessGUDID record 04250676718334
Across registries
- EUDAMED Basic UDI-DI B-04250676718334 registered 30 Sep 2026 Active
- FDA GUDID UDI-DI 04250676718334 listed 5 Oct 2025 Listed
Timeline
- Listed FDA GUDID 04250676718334
- Registered EUDAMED B-04250676718334
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Kerrison sphenoid punch
- Generic name
- Bone-coring punch, reusable
- Device name
- Punches
- Model / Ref / Catalog
- 30-477-20
- Description
- 40° upw., golden tip, totally detachable 2 mm, 23 cm
- Primary DI / UDI-DI
- 04250676718334
- Basic UDI-DI
- B-04250676718334
- FDA product code
- LRC
- EMDN code
- L149012 ENT surgery punches, reusable
- GMDN term
- Bone-coring punch, 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
Manufacturer details
- EUDAMED SRN
- DE-MF-000006647
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