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Heermann gouge 10-726-30

by Spiggle & Theis Medizintechnik GmbH United States GUDID

Product code LRC

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04250381849750 UDI-DIDate14 Sep 2022ListedStatusIn distribution

Coverage

1 jurisdiction

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  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls: none on record (FDA, checked 23 Oct 2026)

Specification

GUDID · synced 23 Oct 2026

Trade Name
Heermann gouge
Generic Name
Mastoid gouge
Model / Ref / Catalog
10-726-30
Primary DI / UDI-DI
04250381849750
FDA Product Code
LRC
GMDN Term
Mastoid gouge
Device Class
Class I
Regulation Number
874.4420
Commercial Distribution
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Related devices

Category: Mastoid gouge

Other devices from Spiggle & Theis Medizintechnik GmbH

See all devices from Spiggle & Theis Medizintechnik GmbH →

Properties & raw data

Show properties, registry sources and raw records
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date
Other properties (10)
  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No

Sources (1)

  • FDA UDI f288a3bd-97b4-421b-bb6d-ef1858d371f8 35 fields · synced 23 Oct 2026