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Hugo

FDA UDI

Class I (US FDA UDI)

by Drive Devilbiss Healthcare

Identity

Trade Name
Hugo FDA UDI
Generic Name
Walking aid handgrip FDA UDI
Device Name
Canes & CrutchesQuad Canes Product Description: HUGO QUADPOD CANE AQUA, 1EA, 6CV, RET. FDA UDI
Model / Reference
731-859 FDA UDI
Description
Canes & CrutchesQuad Canes Product Description: HUGO QUADPOD CANE AQUA, 1EA, 6CV, RET. FDA UDI

Identifiers

Primary DI / UDI-DI
00754021210275 FDA UDI
FDA Product Code
IPS FDA UDI
GMDN Term
Walking aid handgrip FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3075 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Hugo by Drive Devilbiss Healthcare — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c582d0e4-fa74-4a51-a35b-e61e4b900e9a 34 fields · synced Jun 8, 2026