Transcontinental

FDA UDI

Class II (US FDA UDI)

by Globus Medical, Inc.

Identity

Trade Name: TRANSCONTINENTAL FDA UDI
Generic Name: Metallic spinal interbody fusion cage FDA UDI
Device Name: TransContinental Coronal Spacer, 10deg, 18mm x 40mm, 13mm FDA UDI
Model / Reference: 375.594 FDA UDI
Description: TransContinental Coronal Spacer, 10deg, 18mm x 40mm, 13mm FDA UDI

Identifiers

Primary DI / UDI-DI: 00849044081534 FDA UDI
FDA Product Code: MAX FDA UDI
GMDN Term: Metallic spinal interbody fusion cage FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3080 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

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

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Length — 40 Millimeter FDA UDI
Height — 13 Millimeter FDA UDI
Width — 18 Millimeter FDA UDI

Category: Metallic spinal interbody fusion cage

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

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PILLAR TL — Orthofix US LLC · Class II
Solar™ Interbody Fusion System — Degen Medical · Class II
Peridot-TD Anterior Cervical Intervertebral body fusion system — GBS Commonwealth Co., Ltd. · 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: Globus Medical, Inc.

Sources (1)

FDA UDI 0f8e72b3-fe2b-4cca-b1ce-60b970b8b26a 35 fields · synced May 30, 2026