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C-Root 5g

by Beijing C-Root Dental Medical Devices Co., LTD.

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

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 Number06972902580116 UDI-DI Date10 Jun 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
C-Root
Generic Name
Rubber dam, non-latex
Model / Reference
5g
Primary DI / UDI-DI
06972902580116
FDA Product Code
EIE
GMDN Term
Rubber dam, non-latex
Device Class
Class I
Regulation Number
872.6300
GUDID distribution status
In Commercial Distribution

Other devices from Beijing C-Root Dental Medical Devices Co., LTD.

See all devices from Beijing C-Root Dental Medical Devices Co., LTD. →

Properties

  • Premarket Exempt
  • Lot / Batch Number
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (9)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No