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Ezfine Thin Wall Hypodermic Needle 01

by Zhejiang Kindly Medical Devices Co., Ltd.

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 Number06923033459246 UDI-DI Date10 Mar 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  • Withdrawn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

Trade Name
Ezfine Thin Wall Hypodermic Needle
Generic Name
Hypodermic needle, single-use
Model / Ref / Catalog
01, EZF32G13
Primary DI / UDI-DI
06923033459246
510(k) Number
FDA Product Code
FMI
GMDN Term
Hypodermic needle, single-use
Device Class
Class II
Regulation Number
880.5570
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K233037)

Other devices from Zhejiang Kindly Medical Devices Co., Ltd.

See all devices from Zhejiang Kindly Medical Devices Co., Ltd. →

Properties

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

Other properties (9)

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