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Ercp GI114

by Heraeus Medical Components LLC

Ercp GI114 is a Class II device made by Heraeus Medical Components LLC, listed in FDA GUDID since 21 Sep 2016 (UDI-DI 00857834006209), 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 Number00857834006209 UDI-DI Date21 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  • Withdrawn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
Ercp
Generic name
Gastro-urological guidewire, single-use
Model / reference
GI114
Primary DI / UDI-DI
00857834006209
FDA product code
OCY
GMDN term
Gastro-urological guidewire, single-use
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution

Similar devices in this category

Other devices filed under Gastro-urological guidewire, single-use.

Other devices from Heraeus Medical Components LLC

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Properties

  • Supplied sterile
  • Single use
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)