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Demax

FDA UDI

Class II (US FDA UDI)

by Beijing Demax Medical Technology Co., Ltd

Identity

Trade Name
Demax FDA UDI
Generic Name
Rotating pneumatic tourniquet system FDA UDI
Model / Reference
DHD0924 FDA UDI

Identifiers

Primary DI / UDI-DI
06943718225133 FDA UDI
510(k) Number
K222182 FDA UDI
FDA Product Code
DXC FDA UDI
GMDN Term
Rotating pneumatic tourniquet system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4450 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Rotating pneumatic tourniquet system

Demax by Beijing Demax Medical Technology Co., Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rotating pneumatic tourniquet system.

Cleared under the same submission

K222182 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Beijing Demax Medical Technology Co., Ltd

Sources (1)

  • FDA UDI 3c0c0a60-bf49-4004-a165-2215d906bffd 33 fields · synced May 31, 2026