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Sure-Scope C090205

by Obp Corporation

Sure-Scope C090205 is a Class I device made by Obp Corporation, listed in FDA GUDID since 21 Sep 2016 (UDI-DI M648C0902050), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberM648C0902050 UDI-DI Date21 Sep 2016ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Sure-Scope
Generic name
Rigid intubation laryngoscope, reusable
Model / Ref / Catalog
C090205
Primary DI / UDI-DI
M648C0902050
FDA product code
CCW
GMDN term
Rigid intubation laryngoscope, reusable
Device class
Class I
Regulation number
868.5540
GUDID distribution status
In Commercial Distribution

Related devices

Category: Rigid intubation laryngoscope, reusable

Similar devices

Other devices filed under FDA product code CCW (Laryngoscope, Rigid).

Other devices from Obp Corporation

See all devices from Obp Corporation →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)