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CFM Technologies SU-R3

by C F M Technologies Inc

CFM Technologies SU-R3 (LB-SU-R3) is a laryngoscope blade (FDA Class I; FDA product code CCW, Laryngoscope, Rigid) made by C F M Technologies Inc, listed in FDA GUDID since 6 Jan 2020 (UDI-DI 00850013958207), 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 Number00850013958207 UDI-DI Date6 Jan 2020ListedStatusListed 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  • Withdrawn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
CFM Technologies
Generic name
Laryngoscope blade, single-use
Model / Ref / Catalog
SU-R3, LB-SU-R3
Primary DI / UDI-DI
00850013958207
FDA product code
CCW
GMDN term
Laryngoscope blade, single-use
Device class
Class I
Regulation number
868.5540
GUDID distribution status
In Commercial Distribution

Related devices

Category: Laryngoscope blade, single-use

Similar devices in this category

Other devices filed under Laryngoscope blade, single-use.

Other devices from C F M Technologies Inc

See all devices from C F M Technologies Inc →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)