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Fisch dissector 10-655-01 TAN

by Spiggle & Theis Medizintechnik GmbH

Fisch dissector 10-655-01 TAN is a Class I device made by Spiggle & Theis Medizintechnik GmbH, listed in FDA GUDID since 13 Sep 2022 (UDI-DI 04250676716736), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04250676716736 UDI-DI Date13 Sep 2022ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Fisch dissector
Generic name
Open-surgery dissector
Model / Ref / Catalog
10-655-01 TAN
Description
double curved, right 16 cm, black coated
Primary DI / UDI-DI
04250676716736
FDA product code
LRC
GMDN term
Open-surgery dissector
Device class
Class I
Regulation number
874.4420
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Open-surgery dissector

Similar devices in this category

Other devices filed under Open-surgery dissector.

Other devices from Spiggle & Theis Medizintechnik GmbH

See all devices from Spiggle & Theis Medizintechnik GmbH →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)