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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
1" HYSYNAL SYNTHETIC TOURNIQUET STRAPS PERFORATED 25/RL, 4RL/BOX FDA UDI
Model / Reference
14347 FDA UDI
Description
1" HYSYNAL SYNTHETIC TOURNIQUET STRAPS PERFORATED 25/RL, 4RL/BOX FDA UDI

Identifiers

Primary DI / UDI-DI
10087453143475 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
Not 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

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 66c22c43-b418-4cb7-b477-8b532160eb44 35 fields · synced Jun 8, 2026