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Sage TAP LC 7282

by Sage Products LLC

Sage TAP LC 7282 is a Class I device made by Sage Products LLC, listed in FDA GUDID since 26 Mar 2024 (UDI-DI 07613327632880), 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 Number07613327632880 UDI-DI Date26 Mar 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  • Withdrawn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
Sage TAP LC
Generic name
Patient transfer/turning sheet, single-use
Model / Ref / Catalog
7282
Primary DI / UDI-DI
07613327632880
FDA product code
FSA, FMR, KME
GMDN term
Patient transfer/turning sheet, single-use
Device class
Class I
Regulation number
880.5510, 880.6785, 880.6060
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe

Related devices

Category: General-purpose patient lifting system sling/harnessAbsorbent underpad, non-antimicrobial, single-usePatient transfer/turning sheet, single-use

Similar devices

Other devices filed under FDA product code FSA (Lift, patient, non-ac-powered).

Other devices from Sage Products LLC

  • Sage

    Class IIa

  • Sage

    Class I

  • Sage

    Class IIa

  • Sage

    Class I

See all devices from Sage Products LLC →

Properties

  • Single use
  • Over-the-counter
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
Other properties (10, all answered No)