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LifeGlobal® Micropipet

FDA UDI

Class II (US FDA UDI)

by LifeGlobal Group, LLC

Identity

Trade Name
LifeGlobal® Micropipet FDA UDI
Generic Name
Assisted reproduction microtool FDA UDI
Device Name
LG µPipets®: Holding 35° - PINK (1pc) FDA UDI
Model / Reference
MPHL-35*01* FDA UDI
Description
LG µPipets®: Holding 35° - PINK (1pc) FDA UDI

Identifiers

Catalog Number
MPHL-35*01* FDA UDI
Primary DI / UDI-DI
00815965021904 FDA UDI
FDA Product Code
MQJ FDA UDI
GMDN Term
Assisted reproduction microtool FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.6150 FDA UDI
Commercial Distribution
Not 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

Dimensions & Sizes

Size
Outer Diameter — 100 Micrometer FDA UDI
Angle — 35 degree FDA UDI
Lumen/Inner Diameter — 20 Micrometer FDA UDI

LifeGlobal® Micropipet by LifeGlobal Group, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b61d909e-1b87-4975-959e-179a0a996f89 38 fields · synced Jun 9, 2026