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JULIET® Ti

FDA UDI

Class I (US FDA UDI)

by Spineart

Identity

Trade Name
JULIET® Ti FDA UDI
Generic Name
Spinal implant trial FDA UDI
Device Name
TRIAL IMPLANT TI PO/OL SMALL WIDTH L36 W09 H15 FDA UDI
Model / Reference
JUT-IN 08 15-N FDA UDI
Description
TRIAL IMPLANT TI PO/OL SMALL WIDTH L36 W09 H15 FDA UDI

Identifiers

Catalog Number
JUT-IN 08 15-N FDA UDI
Primary DI / UDI-DI
07640332470084 FDA UDI
FDA Product Code
HWT FDA UDI
GMDN Term
Spinal implant trial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4800 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Height — 15 Millimeter FDA UDI
Weight — 9 Gram FDA UDI
Length — 36 Millimeter FDA UDI

Category: Spinal implant trial

JULIET® Ti by Spineart — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal implant trial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Spineart

Sources (1)

  • FDA UDI 866aa221-344c-4f4a-98d5-d7f0cdb47e2b 35 fields · synced Jun 1, 2026