Skip to content

Angeltouch It-04

by Angiplast Private, Ltd.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

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 Number00816967020001 UDI-DI Date19 Sep 2016ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Angeltouch
Generic Name
Basic intravenous administration set, noninvasive
Model / Ref / Catalog
IT-04
Primary DI / UDI-DI
00816967020001
FDA Product Code
LHI
GMDN Term
Basic intravenous administration set, noninvasive
Device Class
Class II
Regulation Number
880.5440
GUDID distribution status
In Commercial Distribution
Size
Length — 150 Centimeter

Related devices

Category: Basic intravenous administration set, noninvasive

Other devices from Angiplast Private, Ltd.

Properties

  • Sterile
  • Single Use
  • Contains Latex
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

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