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Jawz Endomyocardial Biopsy Forceps

FDA UDI

Class II (US FDA UDI)

by Argon Medical Devices, Inc.

Identity

Trade Name
Jawz Endomyocardial Biopsy Forceps FDA UDI
Generic Name
Endomyocardial biopsy forceps, single-use FDA UDI
Device Name
Jawz Endomyocardial Biopsy Forceps 7.5F x 50cm Straight FDA UDI
Model / Reference
190020 FDA UDI
Description
Jawz Endomyocardial Biopsy Forceps 7.5F x 50cm Straight FDA UDI

Identifiers

Catalog Number
190020 FDA UDI
Primary DI / UDI-DI
00886333206704 FDA UDI
510(k) Number
K951447 FDA UDI
FDA Product Code
DWZ FDA UDI
GMDN Term
Endomyocardial biopsy forceps, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4075 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

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: Endomyocardial biopsy forceps, single-use

Jawz Endomyocardial Biopsy Forceps by Argon Medical Devices, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endomyocardial biopsy forceps, single-use.

Cleared under the same submission

K951447 also covers:

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 5588f5b8-1ddf-487f-8aef-c43f9a7fe3de 37 fields · synced Jun 9, 2026