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SafeSplint 16" Short Arm Splint

by Aparata Medical

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860011549505 UDI-DI Date24 Sep 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  • Withdrawn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
SafeSplint
Generic Name
Inflatable extremity splint, single-use
Model / Ref / Catalog
16" Short Arm Splint, 600089
Primary DI / UDI-DI
00860011549505
FDA Product Code
FZF
GMDN Term
Inflatable extremity splint, single-use
Device Class
Class I
Regulation Number
878.3900
GUDID distribution status
In Commercial Distribution
Size
Length — 16 Inch

Other devices from Aparata Medical

Properties

  • Single Use
  • Prescription Use
  • Over-the-Counter
  • Premarket Exempt
  • Lot / Batch Number
  • Serial Number
  • Expiration Date

Other properties (7)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Manufacturing Date: No