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Red Tunica RT-37297

by Rodimedi & Associates, Inc.

Red Tunica RT-37297 is a Class II device made by Rodimedi & Associates, Inc., listed in FDA GUDID since 8 Jan 2024 (UDI-DI 00850036464440), 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 Number00850036464440 UDI-DI Date8 Jan 2024ListedStatusListed 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  • Withdrawn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
Red Tunica
Generic name
Insulin syringe/needle, basic
Model / Ref / Catalog
RT-37297
Primary DI / UDI-DI
00850036464440
FDA product code
FMF
GMDN term
Insulin syringe/needle, basic
Device class
Class II
Regulation number
880.5860
GUDID distribution status
In Commercial Distribution
Size
Needle Gauge — 29 Gauge
Length — 12.7 Millimeter
Total Volume — 1.0 Milliliter

Similar devices

Other devices filed under FDA product code FMF (Syringe, Piston).

Other devices from Rodimedi & Associates, Inc.

See all devices from Rodimedi & Associates, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Over-the-counter
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)