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Na 396-0020

by Yeti Dentalprodukte GmbH

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberEYET3960020 UDI-DI Date17 Apr 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  • Withdrawn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

Generic Name
Dental porcelain/ceramic restoration kit
Model / Ref / Catalog
396-0020
Primary DI / UDI-DI
EYET3960020
FDA Product Code
EIH
GMDN Term
Dental porcelain/ceramic restoration kit
Device Class
Class II
Regulation Number
872.6660
GUDID distribution status
In Commercial Distribution
Sterilization Method
Dry Heat Sterilization
MRI Safety
MR Unsafe

Related devices

Category: Dental porcelain/ceramic restoration kit

Other devices from Yeti Dentalprodukte GmbH

See all devices from Yeti Dentalprodukte GmbH →

Properties

  • Single Use
  • Lot / Batch Number
  • Serial Number
  • Expiration Date

Other properties (10)

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