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SlimLine™

FDA UDI

Class II (US FDA UDI)

by Lumenis

Identity

Trade Name
SlimLine™ FDA UDI
Generic Name
General/multiple surgical laser system beam guide, single-use FDA UDI
Model / Reference
SlimLine™ SIS EZ 365 LP FDA UDI

Identifiers

Primary DI / UDI-DI
07290109144542 FDA UDI
FDA Product Code
GEX FDA UDI
GMDN Term
General/multiple surgical laser system beam guide, single-use 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General/multiple surgical laser system beam guide, single-use

SlimLine™ by Lumenis — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General/multiple surgical laser system beam guide, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Lumenis

Sources (1)

  • FDA UDI 93e8f21a-36c1-43fc-aae1-ea83b9608271 32 fields · synced Jun 1, 2026