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Medi

FDA UDI

Class I (US FDA UDI)

by Medi Manufacturing, Inc.

Identity

Trade Name
MEDI FDA UDI
Generic Name
Elbow orthosis FDA UDI
Device Name
PROTECT EPICO ROM BLACK LEFT LONG FDA UDI
Model / Reference
99451 FDA UDI
Description
PROTECT EPICO ROM BLACK LEFT LONG FDA UDI

Identifiers

Primary DI / UDI-DI
00636257117194 FDA UDI
FDA Product Code
IQI FDA UDI
GMDN Term
Elbow orthosis 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Elbow orthosis

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

Similar devices

Also classified as Elbow orthosis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 93e76f83-9134-4a99-a16d-b9c3bd1d43d1 34 fields · synced Jun 6, 2026