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Injection Needle 22 Gauge

by Ranfac Corp.

Injection Needle 22 Gauge is a Class I device made by Ranfac Corp., listed in FDA GUDID since 10 Aug 2020 (UDI-DI 00857878007965), registry data as of 22 Oct 2026.

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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00857878007965 UDI-DI Date10 Aug 2020ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Injection Needle
Generic name
General-purpose syringe, single-use
Model / Ref / Catalog
22 Gauge
Primary DI / UDI-DI
00857878007965
FDA product code
MDM
GMDN term
General-purpose syringe, single-use
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Size
Needle Gauge — 22 Gauge

Related devices

Category: General-purpose syringe, single-use

Similar devices in this category

Other devices filed under General-purpose syringe, single-use.

Other devices from Ranfac Corp.

See all devices from Ranfac Corp. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)