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ClearLine MD Part#:2126

by Anesthesia Safety Products, LLC

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

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 Number00863193000338 UDI-DI Date23 Sep 2016ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
ClearLine MD
Generic Name
Haemodialysis system air/foam detector
Model / Reference
Part#:2126
Primary DI / UDI-DI
00863193000338
De Novo Number
FDA Product Code
OKL
GMDN Term
Haemodialysis system air/foam detector
Device Class
Class II
Regulation Number
880.5445
GUDID distribution status
In Commercial Distribution

Related devices

Category: Haemodialysis system air/foam detector

Cleared under the same submission (DEN080009)

Other devices from Anesthesia Safety Products, LLC

Properties

  • Prescription Use
  • Lot / Batch Number
  • Serial Number
  • Manufacturing Date

Other properties (10)

  • 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
  • Expiration Date: No