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egger LP/W lacquer, soft, 250 ml

by egger Otoplastik + Labortechnik GmbH GUDID

Listed FDA GUDID listing, not in commercial distribution

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberEGOL307020 UDI-DIDate31 Aug 2022ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

GUDID

Trade Name
egger
Generic Name
Earmould, custom-made
Model / Reference
LP/W lacquer, soft, 250 ml
Primary DI / UDI-DI
EGOL307020
FDA Product Code
ESD
GMDN Term
Earmould, custom-made
Device Class
Class I
Regulation Number
874.3300
GUDID distribution status
Not in Commercial Distribution

Other devices from egger Otoplastik + Labortechnik GmbH

Properties

  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (11)

  • 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
  • Serial Number: No
  • Manufacturing Date: No