Skip to content

Aer-O-Scope Workstation Rev B

by Gi View, Ltd.

Aer-O-Scope Workstation Rev B (MASA0101) is a Class II device made by Gi View, Ltd., listed in FDA GUDID since 1 Aug 2017 (UDI-DI 07290016992007), not in commercial distribution (GUDID) as of 23 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 Number07290016992007 UDI-DI Date1 Aug 2017ListedStatusListed GUDID: not 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  • Withdrawn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
Aer-O-Scope Workstation
Generic name
Flexible video colonoscope, single-use
Model / Ref / Catalog
Rev B, MASA0101
Primary DI / UDI-DI
07290016992007
FDA product code
FDF
GMDN term
Flexible video colonoscope, single-use
Device class
Class II
Regulation number
876.1500
GUDID distribution status
Not in Commercial Distribution

Similar devices

Other devices filed under FDA product code FDF (Colonoscope And Accessories, Flexible/Rigid).

Other devices from Gi View, Ltd.

See all devices from Gi View, Ltd. →

Properties

  • Prescription use
  • Serial number
Other properties (13, all answered No)