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EasyStand

FDA UDI

Class I (US FDA UDI)

by Altimate Medical, Inc.

Identity

Trade Name
EasyStand FDA UDI
Generic Name
Pneumatic stander FDA UDI
Model / Reference
Zing Size 2 FDA UDI

Identifiers

Primary DI / UDI-DI
10858921006109 FDA UDI
FDA Product Code
INQ FDA UDI
GMDN Term
Pneumatic stander FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3760 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

Yes

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

Category: Electric standerPneumatic stander

EasyStand by Altimate Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pneumatic stander.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4599a6f7-f5cb-4c2f-bb64-aa21d35737fb 32 fields · synced Jul 10, 2026