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Monitoring Kit

FDA UDI

Class II (US FDA UDI)

by Argon Medical Devices, Inc.

Identity

Trade Name
Monitoring Kit FDA UDI
Generic Name
Invasive blood pressure transducer set FDA UDI
Device Name
Monitoring Kit FDA UDI
Model / Reference
042920006D FDA UDI
Description
Monitoring Kit FDA UDI

Identifiers

Catalog Number
042920006D FDA UDI
Primary DI / UDI-DI
00886333202003 FDA UDI
FDA Product Code
DRS FDA UDI
GMDN Term
Invasive blood pressure transducer set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2850 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Invasive blood pressure transducer set

Monitoring Kit by Argon Medical Devices, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Invasive blood pressure transducer set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Argon Medical Devices, Inc.

Sources (1)

  • FDA UDI f64f0e1a-03cc-4326-884a-41bf5e532d41 35 fields · synced Jun 9, 2026