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Mod Kit Pulset™

FDA UDI

Class I (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
Mod Kit Pulset™ FDA UDI
Generic Name
Arterial blood sampling kit FDA UDI
Device Name
Mod Kit, Pulset 3cc Syringe 22g x 1" (.7 x 25mm) Safety 25u Balanced Heparin FDA UDI
Model / Reference
3362-91 FDA UDI
Description
Mod Kit, Pulset 3cc Syringe 22g x 1" (.7 x 25mm) Safety 25u Balanced Heparin FDA UDI

Identifiers

Primary DI / UDI-DI
00709078003349 FDA UDI
FDA Product Code
CBT FDA UDI
GMDN Term
Arterial blood sampling kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.1100 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

Yes

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

Mod Kit Pulset™ by Westmed, Inc. — Class I — 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 fa13a117-4818-42d2-ba91-743b51f4efb9 33 fields · synced May 30, 2026