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Medadv

FDA UDI

Class II (US FDA UDI)

by Medas, Inc.

Identity

Trade Name
MEDADV FDA UDI
Generic Name
Radial artery compression device FDA UDI
Device Name
PRESS RADIAL ARTERY TOURNIQUET SIZE LARGE FDA UDI
Model / Reference
M962P20L FDA UDI
Description
PRESS RADIAL ARTERY TOURNIQUET SIZE LARGE FDA UDI

Identifiers

Catalog Number
M962P20L FDA UDI
Primary DI / UDI-DI
00819667020814 FDA UDI
510(k) Number
K142359 FDA UDI
FDA Product Code
DXC FDA UDI
GMDN Term
Radial artery compression device FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4450 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: Radial artery compression device

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

Similar devices

Also classified as Radial artery compression device.

Cleared under the same submission

K142359 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medas, Inc.

Sources (1)

  • FDA UDI 6a303d7e-35fc-487b-9ccd-0a59c141ea37 37 fields · synced Jun 8, 2026