Identity
- Trade Name
- LifeGlobal® Micropipet FDA UDI
- Generic Name
- Assisted reproduction microtool FDA UDI
- Device Name
- LG µPipets®: Holding 30° - PINK (1pc) FDA UDI
- Model / Reference
- MPHL-30*01* FDA UDI
- Description
- LG µPipets®: Holding 30° - PINK (1pc) FDA UDI
Identifiers
- Catalog Number
- MPHL-30*01* FDA UDI
- Primary DI / UDI-DI
- 00815965021911 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
- Angle — 30 degree FDA UDILumen/Inner Diameter — 20 Micrometer FDA UDIOuter Diameter — 100 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- LifeGlobal Group, LLC
Sources (1)
- FDA UDI 67202dde-1332-49cb-b0a0-757ce283b61a 38 fields · synced Jun 9, 2026