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Invacare® Aspirator IRC1135

by Invacare Corp.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None ongoing

1 closed

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00841447198086 UDI-DI Date22 Sep 2026ListedStatusListed GUDID: in commercial distribution

Recalls

1 recall · FDA

    • Terminated Z-2642-2014 FDA Class II initiated 3 Aug 2014

    suction canister lids may have occluded ports.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Invacare® Aspirator
Generic Name
Nasal aspirator, electric
Model / Ref / Catalog
IRC1135
Primary DI / UDI-DI
00841447198086
510(k) Number
FDA Product Code
JCX
GMDN Term
Nasal aspirator, electric
Device Class
Class II
Regulation Number
878.4780
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K042349)

Show all (12)

Other devices from Invacare Corp.

See all devices from Invacare Corp. →

Properties

  • Prescription Use
  • Serial Number
  • Manufacturing Date

Other properties (11)

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