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Mx 02-35 0864

by Meta Biomed Co., Ltd.

Mx 02-35 0864 is a Class I device made by Meta Biomed Co., Ltd., listed in FDA GUDID since 28 Oct 2026 (UDI-DI 08809263708645), registry data as of 12 Nov 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08809263708645 UDI-DI Date28 Oct 2026ListedStatusListed 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  • Withdrawn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
Mx 02-35
Generic name
Synthetic gutta-percha
Model / reference
0864
Primary DI / UDI-DI
08809263708645
FDA product code
EKM
GMDN term
Synthetic gutta-percha
Device class
Class I
Regulation number
872.3850
GUDID distribution status
In Commercial Distribution

Other devices from Meta Biomed Co., Ltd.

See all devices from Meta Biomed Co., Ltd. →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)