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Leg Traction Device MOC-142

FDA UDI

Class I (US FDA UDI)

by Mizuho Corporation

Identity

Trade Name
Leg Traction Device MOC-142 FDA UDI
Generic Name
Surgical traction tensioner FDA UDI
Device Name
Leg Traction Device MOC-142 FDA UDI
Model / Reference
08-051-00 FDA UDI
Description
Leg Traction Device MOC-142 FDA UDI

Identifiers

Catalog Number
08-051-00 FDA UDI
Primary DI / UDI-DI
04946329066708 FDA UDI
FDA Product Code
GDC FDA UDI
GMDN Term
Surgical traction tensioner FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4960 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

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 1655 Millimeter FDA UDI

Category: Surgical traction tensioner

Leg Traction Device MOC-142 by Mizuho Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical traction tensioner.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mizuho Corporation

Sources (1)

  • FDA UDI 41c47626-fb62-4a32-8bdb-559f29de7a98 36 fields · synced May 31, 2026