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Bmi

FDA UDI

Class I (US FDA UDI)

by Blake Manufacturing, Inc.

Identity

Trade Name
BMI FDA UDI
Generic Name
Elbow orthosis FDA UDI
Device Name
Elbow Corrective Orthosis, size Large/Left FDA UDI
Model / Reference
ECO-LL FDA UDI
Description
Elbow Corrective Orthosis, size Large/Left FDA UDI

Identifiers

Catalog Number
ECO-LL FDA UDI
Primary DI / UDI-DI
G088ECOLL0 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

No

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

No

FDA UDI

Category: Elbow orthosis

Bmi by Blake 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 d406d85d-4fd7-4e90-aaae-f6a2e836b448 34 fields · synced Jun 8, 2026