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Ramitec™ 33050

by 3M Deutschland GmbH 2 variants

Ramitec™ 33050 is a Class II device made by 3M Deutschland GmbH, listed in FDA GUDID since 4 Aug 2017 (UDI-DI 04035077000390), 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 Number04035077000390 UDI-DI Date4 Aug 2017ListedStatusListed 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  • Withdrawn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
Ramitec™
Generic name
Polyether dental impression material
Model / Ref / Catalog
33050
Primary DI / UDI-DI
04035077000390
FDA product code
ELW
GMDN term
Polyether dental impression material
Device class
Class II
Regulation number
872.3660
GUDID distribution status
In Commercial Distribution

Related devices

Category: Polyether dental impression material

Other devices from 3M Deutschland GmbH

See all devices from 3M Deutschland GmbH →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)