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Tele Pack 20045030

by Karl Storz SE & CO. KG

Tele Pack 20045030 is a Class II device made by Karl Storz SE & CO. KG, listed in FDA GUDID since 23 Sep 2016 (UDI-DI 04048551272008), 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 Number04048551272008 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  • Withdrawn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

Trade name
Tele Pack
Generic name
Endoscopic light source adaptor
Model / reference
20045030
Primary DI / UDI-DI
04048551272008
FDA product code
GCT
GMDN term
Endoscopic light source adaptor
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Endoscopic light source adaptor

Other devices from Karl Storz SE & CO. KG

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Properties

  • Prescription use
Other properties (14, all answered No)