← Back to catalogue

NormaTec MVP Pro Recovery Package

FDA UDI

Class II (US FDA UDI)

by Normatec Industries, Lp

Identity

Trade Name
NormaTec MVP Pro Recovery Package FDA UDI
Generic Name
Sequential venous compression system FDA UDI
Device Name
MVP Pro Recovery Package - Standard FDA UDI
Model / Reference
MVP Pro Recovery Package - Standard FDA UDI
Description
MVP Pro Recovery Package - Standard FDA UDI

Identifiers

Catalog Number
40400 FDA UDI
Primary DI / UDI-DI
00817369021634 FDA UDI
510(k) Number
K013436 FDA UDI
FDA Product Code
JOW FDA UDI
GMDN Term
Sequential venous compression system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Intermittent venous compression systemSequential venous compression system

NormaTec MVP Pro Recovery Package by Normatec Industries, Lp — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sequential venous compression system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 7ed159a7-4e13-4a42-ae29-052b4150a672 35 fields · synced May 31, 2026