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Nasal probe Starter Kit

FDA UDI

Class II (US FDA UDI)

by Lumenis

Identity

Trade Name
Nasal probe Starter Kit FDA UDI
Generic Name
Laser adaptor FDA UDI
Device Name
Additional DM DIs: 07290109144337 07290109144344 07290109144351 07290109144368 07290109144375 07290109144382 07290109144399 07290109144405 07290109144412 FDA UDI
Model / Reference
14630 FDA UDI
Description
Additional DM DIs: 07290109144337 07290109144344 07290109144351 07290109144368 07290109144375 07290109144382 07290109144399 07290109144405 07290109144412 FDA UDI

Identifiers

Catalog Number
AA2603300 FDA UDI
Primary DI / UDI-DI
07290109141312 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

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: Laser adaptor

Nasal probe Starter Kit 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 0f1abed6-1313-477b-babd-e8c9b14e0980 35 fields · synced May 30, 2026