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Plastcare RIT-4312

by Plastcare USA

Plastcare RIT-4312 is a Class II device made by Plastcare USA, listed in FDA GUDID since 12 Dec 2019 (UDI-DI D915RIT43121), 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 NumberD915RIT43121 UDI-DI Date12 Dec 2019ListedStatusListed 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  • Withdrawn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
Plastcare
Generic name
Sterilization packaging, single-use
Model / reference
RIT-4312
Primary DI / UDI-DI
D915RIT43121
FDA product code
JOJ
GMDN term
Sterilization packaging, single-use
Device class
Class II
Regulation number
880.2800
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe

Similar devices

Other devices filed under FDA product code JOJ (Indicator, Physical/Chemical Sterilization Process).

Other devices from Plastcare USA

See all devices from Plastcare USA →

Properties

  • Single use
  • Lot / batch number
  • Expiration date
Other properties (12, all answered No)