Identity

Trade Name
GSO FDA UDI
Generic Name
Arterial tourniquet, pneumatic FDA UDI
Device Name
Disposable Tourniquet Cuff, Single Bladder, Single Port, Sterile, Super Long Leg, 44X4 in FDA UDI
Model / Reference
GDTC4440SS FDA UDI
Description
Disposable Tourniquet Cuff, Single Bladder, Single Port, Sterile, Super Long Leg, 44X4 in FDA UDI

Identifiers

Primary DI / UDI-DI
06975803530709 FDA UDI
FDA Product Code
KCY FDA UDI
GMDN Term
Arterial tourniquet, pneumatic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.5910 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Arterial tourniquet, pneumatic

Gso by Group Supply Organization Medical Technology(Shanghai) Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arterial tourniquet, pneumatic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 12d0dc2b-f424-4039-999c-a9381be5e2a5 33 fields · synced May 30, 2026