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Joseph placing instrument 20-856-17

by Spiggle & Theis Medizintechnik GmbH

Ref 20-856-17

Joseph placing instrument 20-856-17 is a Class I device made by Spiggle & Theis Medizintechnik GmbH, registered in EUDAMED on 30 Sep 2026 (Basic UDI-DI 425038185G1001RG) and listed in FDA GUDID since 16 Sep 2022 (UDI-DI 04250676733726), active as of 25 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number425038185G1001RG Basic UDI-DI 04250676733726UDI-DIDate30 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04250676733726 UDI-DI Date16 Sep 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 425038185G1001RG registered 30 Sep 2026 Active
  • FDA GUDID UDI-DI 04250676733726 listed 16 Sep 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04250676733726
  2. Registered EUDAMED 425038185G1001RG

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Joseph placing instrument
Generic name
Surgical depth gauge, reusable
Device name
Measuring and Testing Instruments
Model / Ref / Catalog
20-856-17
Description
for rhinoplasty, angled 17 cm
Primary DI / UDI-DI
04250676733726
Basic UDI-DI
425038185G1001RG
Direct marketing DI
04250676733726
FDA product code
JYJ
EMDN code
L149099 ENT instruments, reusable - other
GMDN term
Surgical depth gauge, reusable
Device class
Class I
Regulation number
874.4420
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Surgical depth gauge, reusable

Similar devices in this category

Other devices filed under ENT INSTRUMENTS, REUSABLE - OTHER.

Other devices from Spiggle & Theis Medizintechnik GmbH

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (20, all answered No)