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Hysynal

FDA UDI

Class I (US FDA UDI)

by Hygenic Corporation, The

Identity

Trade Name
Hysynal FDA UDI
Generic Name
Tourniquet cuff, single-use FDA UDI
Device Name
HYSYNAL 1" T-STRAP 4/250 PKG, Synthetic Rubber Tourniquet Strap FDA UDI
Model / Reference
10263 FDA UDI
Description
HYSYNAL 1" T-STRAP 4/250 PKG, Synthetic Rubber Tourniquet Strap FDA UDI

Identifiers

Primary DI / UDI-DI
00087453102635 FDA UDI
FDA Product Code
GAX FDA UDI
GMDN Term
Tourniquet cuff, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.5900 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 18 Inch FDA UDI
Width — 1 Inch FDA UDI

Category: Tourniquet cuff, single-use

Hysynal by Hygenic Corporation, The — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tourniquet cuff, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bd171ef1-bbd9-484e-baf8-8f8a2ca8342f 34 fields · synced Jun 1, 2026