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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
Manual orthopaedic bender, reusable FDA UDI
Device Name
in situ rod bender, right, Ø 6.0mm FDA UDI
Model / Reference
UU052-70-0011 FDA UDI
Description
in situ rod bender, right, Ø 6.0mm FDA UDI

Identifiers

Primary DI / UDI-DI
00814386025522 FDA UDI
510(k) Number
K191932 FDA UDI
FDA Product Code
NKB FDA UDI
GMDN Term
Manual orthopaedic bender, 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Manual orthopaedic bender, reusable

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

Similar devices

Also classified as Manual orthopaedic bender, 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 196ababf-29c7-4a88-8d84-7e774d3a40cd 35 fields · synced Jun 1, 2026