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Rb-365-Tr-Pl

FDA UDI

Class II (US FDA UDI)

by Laser Peripherals Llc.

Identity

Trade Name
RB-365-TR-PL FDA UDI
Generic Name
General/multiple surgical laser system beam guide, reusable FDA UDI
Device Name
365u ReusableTR Compatible Laser Fiber PL FDA UDI
Model / Reference
RB-365-TR-PL FDA UDI
Description
365u ReusableTR Compatible Laser Fiber PL FDA UDI

Identifiers

Catalog Number
RB-365-TR-PL FDA UDI
Primary DI / UDI-DI
00816469020837 FDA UDI
510(k) Number
K011207 FDA UDI
FDA Product Code
GEX FDA UDI
GMDN Term
General/multiple surgical laser system beam guide, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4810 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General/multiple surgical laser system beam guide, reusable

Rb-365-Tr-Pl by Laser Peripherals Llc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General/multiple surgical laser system beam guide, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2c595c0c-73a7-44b5-9972-dd7a7b23f298 35 fields · synced May 30, 2026