ClearLine MD Part#:2240

by Anesthesia Safety Products, LLC

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

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

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00863193000321 UDI-DI	Date23 Sep 2016Listed	StatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

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

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: ClearLine MD
Generic Name: Basic intravenous administration set, noninvasive
Model / Reference: Part#:2240

Primary DI / UDI-DI: 00863193000321
De Novo Number: DEN080009
FDA Product Code: OKL
GMDN Term: Basic intravenous administration set, noninvasive

Device Class: Class II
Regulation Number: 880.5445
GUDID distribution status: In Commercial Distribution

Other devices from Anesthesia Safety Products, LLC

ClearLine MD Part#:2126

Class II
Airpurge

Class II

Properties

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

Other properties (8)

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