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Bruno Vertical Platform Lift (VPL)

FDA UDI

Class II (US FDA UDI)

by Bruno Independent Living Aids, Inc.

Identity

Trade Name
Bruno Vertical Platform Lift (VPL) FDA UDI
Generic Name
Wheelchair/occupant lift FDA UDI
Device Name
Wheelchair Vertical Platform Lift, 53" or 75" lift height standard, 24Vdc Battery Powered with Charger, Commercial, Indoor or Exterior, ASME A18.1 & B355 Code Compliant FDA UDI
Model / Reference
VPL-3300B FDA UDI
Description
Wheelchair Vertical Platform Lift, 53" or 75" lift height standard, 24Vdc Battery Powered with Charger, Commercial, Indoor or Exterior, ASME A18.1 & B355 Code Compliant FDA UDI

Identifiers

Catalog Number
VPL-3353B, VPL-3375B FDA UDI
Primary DI / UDI-DI
00642561000039 FDA UDI
FDA Product Code
PCE FDA UDI
GMDN Term
Wheelchair/occupant lift FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.3930 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

Yes

FDA UDI

Bruno Vertical Platform Lift (VPL) by Bruno Independent Living Aids, Inc. — Class II — 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 a3050fae-e40a-4f5b-a14d-20df63ad5389 36 fields · synced Jun 8, 2026