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Finger Trap, Small

FDA UDI

Class I (US FDA UDI)

by Mizuho Orthopedic Systems, Inc.

Identity

Trade Name
FINGER TRAP, SMALL FDA UDI
Generic Name
Upper-limb traction wrap/trap, reusable FDA UDI
Model / Reference
3344S FDA UDI

Identifiers

Catalog Number
3344S FDA UDI
Primary DI / UDI-DI
00842430111914 FDA UDI
FDA Product Code
KQZ FDA UDI
GMDN Term
Upper-limb traction wrap/trap, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.5890 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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Upper-limb traction wrap/trap, reusable

Finger Trap, Small by Mizuho Orthopedic Systems, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Upper-limb traction wrap/trap, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a81947dc-8c78-4c49-81b4-97984fa0d0da 34 fields · synced Jun 9, 2026