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Momentum

FDA UDI

Class II (US FDA UDI)

by Ulrich Medical Usa, Inc.

Identity

Trade Name
Momentum FDA UDI
Generic Name
Surgical torque wrench, reusable FDA UDI
Device Name
T-Handle with torque limitation, 6Nm, for crosslinks, coupling H FDA UDI
Model / Reference
UU052-20-0103 FDA UDI
Description
T-Handle with torque limitation, 6Nm, for crosslinks, coupling H FDA UDI

Identifiers

Primary DI / UDI-DI
00814386024976 FDA UDI
510(k) Number
K191932 FDA UDI
FDA Product Code
NKB FDA UDI
GMDN Term
Surgical torque wrench, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical torque wrench, reusable

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

Similar devices

Also classified as Surgical torque wrench, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 99aec0b9-b56e-457a-8498-e65c973124a3 35 fields · synced Jun 8, 2026