Medi

FDA UDI

Class I (US FDA UDI)

by Medi Manufacturing, Inc.

Identity

Trade Name: MEDI FDA UDI
Generic Name: Compression/pressure sock/stocking, single-use FDA UDI
Device Name: COMFORT ARM 15-20 STD SAND V FDA UDI
Model / Reference: CA10285 FDA UDI
Description: COMFORT ARM 15-20 STD SAND V FDA UDI

Identifiers

Primary DI / UDI-DI: 00636257009086 FDA UDI
FDA Product Code: ILG FDA UDI
GMDN Term: Compression/pressure sock/stocking, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 890.3475 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Compression/pressure sock/stocking, single-use

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Medi Manufacturing, Inc.

Sources (1)

FDA UDI 4438e3ac-2865-41ab-ae55-a99bf59582bc 34 fields · synced Jul 31, 2026