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PrepEM Wild 18in splint

by Emsrun Group

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 Number06975675781490 UDI-DI Date7 Nov 2025ListedStatusListed GUDID: 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  • Withdrawn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
PrepEM Wild
Generic Name
First aid limb splint, mouldable, single-use
Model / Reference
18in splint
Primary DI / UDI-DI
06975675781490
FDA Product Code
HSP
GMDN Term
First aid limb splint, mouldable, single-use
Device Class
Class I
Regulation Number
888.5890
GUDID distribution status
In Commercial Distribution

Other devices from Emsrun Group

See all devices from Emsrun Group →

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