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Regard™ TM1522REG

by Resource Optimization & Innovation, L.L.C.

Regard™ TM1522REG is a Class I device made by Resource Optimization & Innovation, L.L.C., listed in FDA GUDID since 21 Nov 2025 (UDI-DI 30326053102791), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number30326053102791 UDI-DI Date21 Nov 2025ListedStatusListed 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  • Withdrawn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
Regard™
Generic name
Endoscopic insufflation tubing set, single-use
Model / Ref / Catalog
TM1522REG
Primary DI / UDI-DI
30326053102791
FDA product code
NKC
GMDN term
Endoscopic insufflation tubing set, single-use
Device class
Class I
Regulation number
884.1730
GUDID distribution status
In Commercial Distribution

Other devices from Resource Optimization & Innovation, L.L.C.

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)