Movement®

FDA UDI

Class I (US FDA UDI)

by Ascension Orthopedics, Inc.

Identity

Trade Name: Movement® FDA UDI
Generic Name: Orthopaedic broach FDA UDI
Device Name: Movement® Great Toe System Proximal Phalanx Broach The Movement Great Toe Proximal Phalanx Broach is used to prepare a cavity that provides a press fit for the implant. FDA UDI
Model / Reference: PPB-890-00 FDA UDI
Description: Movement® Great Toe System Proximal Phalanx Broach The Movement Great Toe Proximal Phalanx Broach is used to prepare a cavity that provides a press fit for the implant. FDA UDI

Identifiers

Catalog Number: PPB89000 FDA UDI
Primary DI / UDI-DI: 10381780246664 FDA UDI
FDA Product Code: HTQ FDA UDI
GMDN Term: Orthopaedic broach FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.4540 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

Yes

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Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic broach

Movement® by Ascension Orthopedics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: Ascension Orthopedics, Inc.

Sources (1)

FDA UDI cd7a703d-7e0e-4d8b-aecc-55a164707a8a 37 fields · synced May 29, 2026