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Medi

FDA UDI

Class I (US FDA UDI)

by Medi Manufacturing, Inc.

Identity

Trade Name
MEDI FDA UDI
Generic Name
Compression bandaging kit FDA UDI
Device Name
JUXTAFIT ESSENTIALS BLK 36CM XL FDA UDI
Model / Reference
CJF33504 FDA UDI
Description
JUXTAFIT ESSENTIALS BLK 36CM XL FDA UDI

Identifiers

Primary DI / UDI-DI
00636257096697 FDA UDI
FDA Product Code
MDR FDA UDI
GMDN Term
Compression bandaging kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5160 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: Compression bandaging kit

A comprehensive medical device directory, featuring a cutting-edge compression bandaging kit designed to provide graduated ascending-decreasing compression for the treatment of venous leg ulcers and related conditions. Our MEDI Compression Bandaging Kit is carefully crafted with sequential application layers to ensure optimal pressure relief.

Similar devices

Also classified as Compression bandaging kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medi Manufacturing, Inc.

Sources (1)

  • FDA UDI 6bb670a7-2d18-490d-b3a8-02d1a731d3df 34 fields · synced Jul 26, 2026