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Delfin RIIDSMMIC

by Intra-Lock International

Delfin RIIDSMMIC is a Class I device made by Intra-Lock International, listed in FDA GUDID since 11 Jul 2019 (UDI-DI D742RIIDSMMIC0), 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 NumberD742RIIDSMMIC0 UDI-DI Date11 Jul 2019ListedStatusListed 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  • Withdrawn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
Delfin
Generic name
Dental power tool system handpiece, line-powered
Model / Ref / Catalog
RIIDSMMIC
Primary DI / UDI-DI
D742RIIDSMMIC0
FDA product code
EFA
GMDN term
Dental power tool system handpiece, line-powered
Device class
Class I
Regulation number
872.4200
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code EFA (Handpiece, Belt And/Or Gear Driven, Dental).

Other devices from Intra-Lock International

See all devices from Intra-Lock International →

Properties

  • Prescription use
  • Lot / batch number
Other properties (13, all answered No)