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Monument

FDA UDI

Class I (US FDA UDI)

by Globus Medical, Inc.

Identity

Trade Name
MONUMENT FDA UDI
Generic Name
Orthopaedic rod reducer FDA UDI
Device Name
MONUMENT DTS Guide, Medial, 15mm FDA UDI
Model / Reference
6108.3015 FDA UDI
Description
MONUMENT DTS Guide, Medial, 15mm FDA UDI

Identifiers

Primary DI / UDI-DI
00889095171006 FDA UDI
510(k) Number
K132559 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic rod reducer 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Dimensions & Sizes

Size
Height — 15 Millimeter FDA UDI

Category: Orthopaedic rod reducer

Monument by Globus Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic rod reducer.

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 06e6a933-e049-4ec5-a320-bd0f5c6a3d5e 36 fields · synced May 30, 2026