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Lingo 78782-01

by Abbott Diabetes Care Inc

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00357599850005 UDI-DI Date17 Nov 2025ListedStatusListed 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  • Withdrawn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
Lingo
Generic Name
Percutaneous interstitial fluid glucose monitoring system, electrochemical
Model / Ref / Catalog
78782-01
Primary DI / UDI-DI
00357599850005
FDA Product Code
SAF
GMDN Term
Percutaneous interstitial fluid glucose monitoring system, electrochemical
Device Class
Class II
Regulation Number
862.1355
GUDID distribution status
In Commercial Distribution

Other devices from Abbott Diabetes Care Inc

See all devices from Abbott Diabetes Care Inc →

Properties

  • Sterile
  • Single Use
  • Over-the-Counter

Other properties (11)

  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No