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Gaesca

FDA UDI

Class I (US FDA UDI)

by Mp2g Diagnostic Corp

Identity

Trade Name
GAESCA FDA UDI
Generic Name
Axillary crutch FDA UDI
Device Name
Aluminium Basic Crutches Size M (Pair) FDA UDI
Model / Reference
Gaesca Aluminium Basic Crutches M FDA UDI
Description
Aluminium Basic Crutches Size M (Pair) FDA UDI

Identifiers

Primary DI / UDI-DI
00850051333059 FDA UDI
FDA Product Code
IPR FDA UDI
GMDN Term
Axillary crutch FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3150 FDA UDI
Commercial Distribution
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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Axillary crutch

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

Similar devices

Also classified as Axillary crutch.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2bccbc38-d12c-42ca-98df-8dc9558aa30a 33 fields · synced May 31, 2026