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Hariomed culture dish TLdish-2*8

by Hua Yue Medical Technology 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 Number06975183900017 UDI-DI Date30 Sep 2025ListedStatusListed 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  • Withdrawn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
Hariomed culture dish
Generic Name
Assisted reproduction procedure dish
Model / Reference
TLdish-2*8
Primary DI / UDI-DI
06975183900017
510(k) Number
FDA Product Code
MQK
GMDN Term
Assisted reproduction procedure dish
Device Class
Class II
Regulation Number
884.6160
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K242684)

Other devices from Hua Yue Medical Technology Co., Ltd.

See all devices from Hua Yue Medical Technology Co., Ltd. →

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