DA Power Hook

FDA UDI

Class I (US FDA UDI)

by United Orthopedic Corp.

Identity

Trade Name: DA Power Hook FDA UDI
Generic Name: Femur lifter, electric FDA UDI
Device Name: Power hook set FDA UDI
Model / Reference: 9909-5601-RA FDA UDI
Description: Power hook set FDA UDI

Identifiers

Catalog Number: 9909-5601-RA FDA UDI
Primary DI / UDI-DI: 04719886905434 FDA UDI
FDA Product Code: JEA FDA UDI
GMDN Term: Femur lifter, electric 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Foot-switch, electrical Femur lifter, electric

DA Power Hook by United Orthopedic Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Femur lifter, electric.

Adante Femur Lift — Mizuho Orthopedic Systems, Inc. · Class I
ASSEMBLY, FEMUR LIFT LH, REFURBISHED — Mizuho Orthopedic Systems, Inc. · Class I
ASSEMBLY, FEMUR LIFT RH, REFURBISHED — Mizuho Orthopedic Systems, Inc. · Class I
Adante Femoral Hook Bracket — Mizuho Orthopedic Systems, Inc. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: United Orthopedic Corp.

Sources (1)

FDA UDI 14c21b54-0ab3-4be5-bff0-038cad187a89 35 fields · synced May 31, 2026