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CoreCare

by Corecare Products Inc. 20 variants

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850091070051 UDI-DI Date11 Sep 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic Name
Insulin syringe/needle, basic
Model / Reference
Insulin Syringe, double cap, 1ml, 30GX5/16''
Description
Insulin Syringe, double cap, 1ml,30GX5/16''
Primary DI / UDI-DI
00850091070051
510(k) Number
FDA Product Code
FMI
GMDN Term
Insulin syringe/needle, basic
Device Class
Class II
Regulation Number
880.5570
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K202570)

Show all (12)

Other devices from Corecare Products Inc.

See all devices from Corecare Products Inc. →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No