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Pulset

FDA UDI

Class II (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
Pulset FDA UDI
Generic Name
Arterial blood sampling kit FDA UDI
Device Name
Pulset 3cc Syringe 23g x 1" (.6 x 25mm) Crickett 25u Balanced Heparin (Chinese Labels) FDA UDI
Model / Reference
3303-95+ FDA UDI
Description
Pulset 3cc Syringe 23g x 1" (.6 x 25mm) Crickett 25u Balanced Heparin (Chinese Labels) FDA UDI

Identifiers

Primary DI / UDI-DI
00709078013966 FDA UDI
FDA Product Code
JKA FDA UDI
GMDN Term
Arterial blood sampling kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1675 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Arterial blood sampling kit

Pulset by Westmed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arterial blood sampling kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Westmed, Inc.

Sources (1)

  • FDA UDI 307df9d3-df8d-4e08-9991-4fbb3e86d90d 33 fields · synced May 31, 2026