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Hugo 731-456

by Drive Devilbiss Healthcare GUDID

Withdrawn United States

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00754021211012 UDI-DIDate21 Jun 2019ListedStatusWithdrawn

Coverage

1 jurisdiction

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  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
Hugo
Generic Name
Walking aid handgrip
Model / Reference
731-456
Primary DI / UDI-DI
00754021211012
FDA Product Code
IPS
GMDN Term
Walking aid handgrip
Device Class
Class I
Regulation Number
890.3075
Commercial Distribution
Not in Commercial Distribution

Other devices from Drive Devilbiss Healthcare

See all devices from Drive Devilbiss Healthcare →

Properties

  • Premarket Exempt
  • Serial Number

Other properties (12)

  • 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
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No