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Namic DYNJSYRPC20P

by Medline Industries, Inc.

Namic DYNJSYRPC20P is a Class II device made by Medline Industries, Inc., listed in FDA GUDID since 14 Aug 2025 (UDI-DI 10889942653706), 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 Number10889942653706 UDI-DI Date14 Aug 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  • Withdrawn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
Namic
Generic name
General-purpose syringe, single-use
Model / Ref / Catalog
DYNJSYRPC20P
Primary DI / UDI-DI
10889942653706
FDA product code
FMF
GMDN term
General-purpose syringe, single-use
Device class
Class II
Regulation number
880.5860
GUDID distribution status
In Commercial Distribution

Related devices

Category: General-purpose syringe, single-use

Similar devices in this category

Other devices filed under General-purpose syringe, single-use.

Other devices from Medline Industries, Inc.

See all devices from Medline Industries, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)