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Ruthless Spine Straight Probe, reusable

FDA UDI

Class II (US FDA UDI)

by Ruthless Spine

Identity

Trade Name
Ruthless Spine Straight Probe, reusable FDA UDI
Generic Name
Abdominal/ENT/orthopaedic surgical probe, reusable FDA UDI
Device Name
RJB system instrument, Straight Probe, reusable FDA UDI
Model / Reference
RJB-PRB1-R FDA UDI
Description
RJB system instrument, Straight Probe, reusable FDA UDI

Identifiers

Catalog Number
RJBPRB1R FDA UDI
Primary DI / UDI-DI
G492RJBPRB1R0 FDA UDI
FDA Product Code
QWL FDA UDI
GMDN Term
Abdominal/ENT/orthopaedic surgical probe, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.4560 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

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

Category: Abdominal/ENT/orthopaedic surgical probe, reusable

Ruthless Spine Straight Probe, reusable by Ruthless Spine — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Abdominal/ENT/orthopaedic surgical probe, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ruthless Spine

Sources (1)

  • FDA UDI 45c61ff8-6e5a-4e9a-8a72-f367dbf87f2f 35 fields · synced Jun 8, 2026