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GlobTek

FDA UDI

Class II (US FDA UDI)

by Microlight Corporation Of America

Identity

Trade Name
GlobTek FDA UDI
Generic Name
Isolation transformer FDA UDI
Device Name
Transformer with Output Cord FDA UDI
Model / Reference
ML-830-02-004 FDA UDI
Description
Transformer with Output Cord FDA UDI

Identifiers

Catalog Number
ML-830-02-004 FDA UDI
Primary DI / UDI-DI
00859626006121 FDA UDI
FDA Product Code
NHN FDA UDI
GMDN Term
Isolation transformer 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: Isolation transformer

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

Similar devices

Also classified as Isolation transformer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Microlight Corporation Of America

Sources (1)

  • FDA UDI d3493557-09da-4e2b-aaf1-754d4735b27e 35 fields · synced May 30, 2026