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Na 163005630

by Medos International Sàrl

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 Number10705034507408 UDI-DI Date13 Oct 2016ListedStatusListed 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  • Withdrawn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

Generic Name
Surgical/emergency suction cannula, non-illuminating, single-use
Model / Ref / Catalog
163005630
Primary DI / UDI-DI
10705034507408
510(k) Number
FDA Product Code
HRX
GMDN Term
Surgical/emergency suction cannula, non-illuminating, single-use
Device Class
Class II
Regulation Number
888.1100
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical/emergency suction cannula, non-illuminating, single-use

Cleared under the same submission (K122861)

Other devices from Medos International SARL

See all devices from Medos International SARL →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No