Skip to content

Polycarbonate Syringe

by Dmc Medical Limited 43 variants

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

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 Number05391530754118 UDI-DI Date27 Sep 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Generic Name
General-purpose syringe, reusable
Model / Ref / Catalog
FD-1068NS 3ml PC Syringe Red Plunger Nitro Print
Primary DI / UDI-DI
05391530754118
510(k) Number
FDA Product Code
FMF
GMDN Term
General-purpose syringe, reusable
Device Class
Class II
Regulation Number
880.5860
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K103736)

Show all (12)

Other devices from Dmc Medical Limited

See all devices from Dmc Medical Limited →

Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number

Other properties (11)

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