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Denver Splint 00812185030136

by Shippert Medical Technologies Corp.

Listed FDA GUDID listing, not in commercial distribution

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00812185030136 UDI-DI Date20 Sep 2018ListedStatusListed GUDID: not 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  • Withdrawn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
Denver Splint
Generic Name
External nasal splint
Model / Reference
00812185030136
Primary DI / UDI-DI
00812185030136
FDA Product Code
EPP
GMDN Term
External nasal splint
Device Class
Class I
Regulation Number
874.5800
GUDID distribution status
Not in Commercial Distribution

Other devices from Shippert Medical Technologies Corp.

See all devices from Shippert Medical Technologies Corp. →

Properties

  • Single Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (9)

  • Sterile: 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