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M-Catch 1175-01

by Diversatek Healthcare

M-Catch 1175-01 is a Class I device made by Diversatek Healthcare, listed in FDA GUDID since 6 Aug 2018 (UDI-DI 00816734021361), 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 Number00816734021361 UDI-DI Date6 Aug 2018ListedStatusListed 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  • Withdrawn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
M-Catch
Generic name
Gastrointestinal/airway foreign body retrieval basket, single-use
Model / Ref / Catalog
1175-01
Primary DI / UDI-DI
00816734021361
FDA product code
FGX
GMDN term
Gastrointestinal/airway foreign body retrieval basket, single-use
Device class
Class I
Regulation number
876.4730
GUDID distribution status
In Commercial Distribution
Size
Width — 3 Centimeter
Depth — 6 Centimeter
Length — 230 Centimeter

Related devices

Category: Gastrointestinal/airway foreign body retrieval basket, single-use

Similar devices in this category

Other devices filed under Gastrointestinal/airway foreign body retrieval basket, single-use.

Other devices from Diversatek Healthcare

See all devices from Diversatek Healthcare →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)