Gaesca

FDA UDI

Class I (US FDA UDI)

by Mp2g Diagnostic Corp

Identity

Trade Name: GAESCA FDA UDI
Generic Name: Push-rim manual wheelchair, bariatric FDA UDI
Device Name: Standard Wheelchair armrest and footrest removable 120 kgs/264lbs weight capacity for overweight people and bariatric use FDA UDI
Model / Reference: Gaesca Standard Wheelchair armrest footrest removable 264lbs/120kgs FDA UDI
Description: Standard Wheelchair armrest and footrest removable 120 kgs/264lbs weight capacity for overweight people and bariatric use FDA UDI

Identifiers

Primary DI / UDI-DI: 00850051333073 FDA UDI
FDA Product Code: INM FDA UDI
GMDN Term: Push-rim manual wheelchair, bariatric FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 890.3100 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Push-rim manual wheelchair, bariatric

Gaesca by Mp2g Diagnostic Corp — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Mp2g Diagnostic Corp

Sources (1)

FDA UDI 9bbbeade-03c4-441a-a148-2d15c55ad584 33 fields · synced Jun 8, 2026