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Pioneer IVF®

FDA UDI

Class II (US FDA UDI)

by LifeGlobal Group, LLC

Identity

Trade Name
Pioneer IVF® FDA UDI
Generic Name
General-purpose suction system, line-powered FDA UDI
Device Name
Propump Single 230V FDA UDI
Model / Reference
GPPS-230 FDA UDI
Description
Propump Single 230V FDA UDI

Identifiers

Catalog Number
GPPS-230 FDA UDI
Primary DI / UDI-DI
00815965021683 FDA UDI
510(k) Number
K914220 FDA UDI
FDA Product Code
HHK FDA UDI
GMDN Term
General-purpose suction system, line-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1175 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General-purpose suction system, line-powered

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

Similar devices

Also classified as General-purpose suction system, line-powered.

Cleared under the same submission

K914220 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 71d95ae2-a992-4135-8f87-47a551f81cba 37 fields · synced Jun 9, 2026