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ri-integral set Macintosh LED 2.5 V, with C-handle 8041

by Rudolf Riester GmbH & Co. KG

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04045396168282 UDI-DI Date28 Jan 2021ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
ri-integral set Macintosh LED 2.5 V, with C-handle
Generic Name
Rigid intubation laryngoscope, reusable
Model / Ref / Catalog
8041
Primary DI / UDI-DI
04045396168282
510(k) Number
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

Cleared under the same submission (K945425)

Show all (12)

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Properties

  • Lot / Batch Number
  • Manufacturing Date

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No