← Back to catalogue

Knee Foot Support Liner

FDA UDI

Class I (US FDA UDI)

by Mizuho Orthopedic Systems, Inc.

Identity

Trade Name
KNEE FOOT SUPPORT LINER FDA UDI
Generic Name
Orthopaedic knee/leg holder liner FDA UDI
Model / Reference
6895-1223 FDA UDI

Identifiers

Primary DI / UDI-DI
00842430116452 FDA UDI
FDA Product Code
FMP FDA UDI
GMDN Term
Orthopaedic knee/leg holder liner FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6450 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthopaedic knee/leg holder liner

Knee Foot Support Liner by Mizuho Orthopedic Systems, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic knee/leg holder liner.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 20f59fa2-f9d3-4131-b632-4fe1eb5a9d96 33 fields · synced Jun 9, 2026