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27147X-S

by Karl Storz SE & CO. KG

27147X-S is a Class II device made by Karl Storz SE & CO. KG, listed in FDA GUDID since 23 Sep 2016 (UDI-DI 04048551395714), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04048551395714 UDI-DI Date23 Sep 2016ListedStatusListed 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  • Withdrawn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

Generic name
Scalpel, reusable
Model / reference
27147X-S
Primary DI / UDI-DI
04048551395714
FDA product code
EZO
GMDN term
Scalpel, reusable
Device class
Class II
Regulation number
876.4770
GUDID distribution status
In Commercial Distribution

Related devices

Category: Scalpel, reusable

Similar devices in this category

Other devices filed under Scalpel, reusable.

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)