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Romeo 2 Instrumentation

FDA UDI

Class I (US FDA UDI)

by Spineart

Identity

Trade Name
ROMEO 2 INSTRUMENTATION FDA UDI
Generic Name
Orthopaedic rod reducer FDA UDI
Device Name
RIBAC L FDA UDI
Model / Reference
SPE-IN 01 43-N FDA UDI
Description
RIBAC L FDA UDI

Identifiers

Catalog Number
SPE-IN 01 43-N FDA UDI
Primary DI / UDI-DI
07640178980815 FDA UDI
FDA Product Code
HXW FDA UDI
GMDN Term
Orthopaedic rod reducer FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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: Orthopaedic rod reducer

Romeo 2 Instrumentation by Spineart — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic rod reducer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Spineart

Sources (1)

  • FDA UDI ca428d1a-7d0f-4676-ba77-6028de6b6c48 34 fields · synced May 30, 2026