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BeamAlign Laparoscope Coupler 300mm

FDA UDI

Class II (US FDA UDI)

by Lumenis

Identity

Trade Name
BeamAlign Laparoscope Coupler 300mm FDA UDI
Generic Name
Laser adaptor FDA UDI
Model / Reference
BeamAlign Laparoscope Coupler 300mm FDA UDI

Identifiers

Catalog Number
AA2330600 FDA UDI
Primary DI / UDI-DI
07290109141855 FDA UDI
FDA Product Code
GEX FDA UDI
GMDN Term
Laser adaptor 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Laser adaptor

BeamAlign Laparoscope Coupler 300mm by Lumenis — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laser adaptor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Lumenis

Sources (1)

  • FDA UDI 53e25bd7-a56f-483c-a1ac-16a1694df0ed 34 fields · synced May 30, 2026