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Medadv

FDA UDI

Class II (US FDA UDI)

by Medas, Inc.

Identity

Trade Name
MEDADV FDA UDI
Generic Name
Peripheral vascular catheter FDA UDI
Device Name
PERIPHERAL INTRAVENOUS CATHETER 20G X 1.3" FDA UDI
Model / Reference
M202 FDA UDI
Description
PERIPHERAL INTRAVENOUS CATHETER 20G X 1.3" FDA UDI

Identifiers

Catalog Number
M202 FDA UDI
Primary DI / UDI-DI
00819667020210 FDA UDI
510(k) Number
K070451 FDA UDI
FDA Product Code
FOZ FDA UDI
GMDN Term
Peripheral vascular catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5200 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: Peripheral vascular catheter

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

Similar devices

Also classified as Peripheral vascular catheter.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medas, Inc.

Sources (1)

  • FDA UDI 7d8694c6-d537-4fc6-bd3c-641e4e09e51d 37 fields · synced May 30, 2026