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Ml 830®

FDA UDI

Class II (US FDA UDI)

by Microlight Corporation Of America

Identity

Trade Name
ML 830® FDA UDI
Generic Name
Laser beam delivery unit holder FDA UDI
Device Name
SL Triple Probe Holder FDA UDI
Model / Reference
ML-830-07-007 FDA UDI
Description
SL Triple Probe Holder FDA UDI

Identifiers

Catalog Number
ML-830-07-007 FDA UDI
Primary DI / UDI-DI
00859626006312 FDA UDI
FDA Product Code
NHN FDA UDI
GMDN Term
Laser beam delivery unit holder FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5500 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

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Laser beam delivery unit holder

Ml 830® by Microlight Corporation Of America — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laser beam delivery unit holder.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1b8c39ff-7b24-4da4-ba8a-304c3e423920 35 fields · synced May 30, 2026