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Sustain

FDA UDI

Class II (US FDA UDI)

by Globus Medical, Inc.

Identity

Trade Name
SUSTAIN FDA UDI
Generic Name
Metallic spinal interbody fusion cage FDA UDI
Device Name
SUSTAIN Spacer, Medium, 12mm, Parallel FDA UDI
Model / Reference
101.212 FDA UDI
Description
SUSTAIN Spacer, Medium, 12mm, Parallel FDA UDI

Identifiers

Primary DI / UDI-DI
00849044078046 FDA UDI
FDA Product Code
ODP FDA UDI
MQP FDA UDI
GMDN Term
Metallic spinal interbody fusion cage FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3080 FDA UDI
888.3060 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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
Depth — 13 Millimeter FDA UDI
Height — 12 Millimeter FDA UDI
Width — 14 Millimeter FDA UDI

Category: Metallic spinal interbody fusion cage

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

Similar devices

Also classified as Metallic spinal interbody fusion cage.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 15fefd53-60be-4295-9ef0-bb50fa470060 35 fields · synced May 30, 2026