← Back to catalogue

Medi

FDA UDI

Class II (US FDA UDI)

by Medi Manufacturing, Inc.

Identity

Trade Name
MEDI FDA UDI
Generic Name
Single-chamber venous compression system garment, single-use FDA UDI
Device Name
MEDI PCS 6 CH LOWER LEG BLK SM 20 FDA UDI
Model / Reference
CSLL065S20 FDA UDI
Description
MEDI PCS 6 CH LOWER LEG BLK SM 20 FDA UDI

Identifiers

Primary DI / UDI-DI
00636257002063 FDA UDI
FDA Product Code
JOW FDA UDI
GMDN Term
Single-chamber venous compression system garment, single-use 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

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Single-chamber venous compression system garment, single-use

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

Similar devices

Also classified as Single-chamber venous compression system garment, single-use.

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

Manufacturer
Medi Manufacturing, Inc.

Sources (1)

  • FDA UDI b182425c-7def-4432-b315-a7594753a35f 34 fields · synced May 31, 2026