Momentum

FDA UDI

Class II (US FDA UDI)

by Ulrich Medical Usa, Inc.

Identity

Trade Name: Momentum FDA UDI
Generic Name: Orthopaedic stereotactic surgery system FDA UDI
Device Name: Navigated screwdriver for reduction screws, SR20, 1/4"-square FDA UDI
Model / Reference: UU062-83-0103 FDA UDI
Description: Navigated screwdriver for reduction screws, SR20, 1/4"-square FDA UDI

Identifiers

Primary DI / UDI-DI: 00814386025799 FDA UDI
FDA Product Code: NKB FDA UDI
OLO FDA UDI
GMDN Term: Orthopaedic stereotactic surgery system FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3070 FDA UDI
882.4560 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

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

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Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic stereotactic surgery system

Momentum by Ulrich Medical Usa, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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WatchTower — Intai Technology Corporation · Class II

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 II	Pending data

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Manufacturer

Manufacturer: Ulrich Medical Usa, Inc.

Sources (1)

FDA UDI 4533085c-8274-4d04-a158-71017b6dba1d 34 fields · synced May 30, 2026