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Panacea

FDA UDI

Class I (US FDA UDI)

by Blake Manufacturing, Inc.

Identity

Trade Name
Panacea FDA UDI
Generic Name
Knee support orthosis FDA UDI
Device Name
Panacea Knee Corrective orthosis, size Petite/Right FDA UDI
Model / Reference
DS-KCO-PR FDA UDI
Description
Panacea Knee Corrective orthosis, size Petite/Right FDA UDI

Identifiers

Catalog Number
DS-KCO-PR FDA UDI
Primary DI / UDI-DI
G088DSKCOPR0 FDA UDI
FDA Product Code
ITQ FDA UDI
GMDN Term
Knee support 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: Knee support orthosis

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

Similar devices

Also classified as Knee support orthosis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 67384cf9-695d-4522-8fc2-9f64266a3258 34 fields · synced Jun 1, 2026