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Juliet Instrumentation

FDA UDI

Class I (US FDA UDI)

by Spineart

Identity

Trade Name
JULIET INSTRUMENTATION FDA UDI
Generic Name
Bone lever/elevator, reusable FDA UDI
Device Name
UP ANGLE COBB 17MM FDA UDI
Model / Reference
JLL-IN 01 04-N FDA UDI
Description
UP ANGLE COBB 17MM FDA UDI

Identifiers

Catalog Number
JLL-IN 01 04-N FDA UDI
Primary DI / UDI-DI
07640178982833 FDA UDI
FDA Product Code
FZS FDA UDI
GMDN Term
Bone lever/elevator, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Category: Bone lever/elevator, reusable

Juliet Instrumentation by Spineart — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone lever/elevator, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Spineart

Sources (1)

  • FDA UDI 09d70183-c2e0-466e-a782-9ba70b9ecb3a 34 fields · synced May 31, 2026