Juliet® OL Transforaminal Lumbar Cage

FDA UDI

Class II (US FDA UDI)

by Spineart

Identity

Trade Name: Juliet® OL Transforaminal Lumbar Cage FDA UDI
Generic Name: Polymeric spinal fusion cage, sterile FDA UDI
Device Name: Straight Transforaminal Lumbar Cage Lordotic FDA UDI
Model / Reference: JUL-OX 32 08-S FDA UDI
Description: Straight Transforaminal Lumbar Cage Lordotic FDA UDI

Identifiers

Catalog Number: JUL-OX 32 08-S FDA UDI
Primary DI / UDI-DI: 07640151087265 FDA UDI
FDA Product Code: MAX FDA UDI
GMDN Term: Polymeric spinal fusion cage, sterile 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size: Angle — 12 degree FDA UDI
Height — 08 Millimeter FDA UDI
Length — 32 Millimeter FDA UDI

Category: Polymeric spinal fusion cage, sterile

Juliet® OL Transforaminal Lumbar Cage by Spineart — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: Spineart

Sources (1)

FDA UDI 6ec061d8-9995-4883-923c-fea542225d74 35 fields · synced May 30, 2026