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MedPak

FDA UDI

Class II (US FDA UDI)

by Lifeport, Llc.

Identity

Trade Name
MedPak FDA UDI
Generic Name
Laboratory pump, vacuum FDA UDI
Device Name
MEDPAK ASSEMBLY, LOW PROFILE FDA UDI
Model / Reference
MP2-009-07-A1B1C1D1 FDA UDI
Description
MEDPAK ASSEMBLY, LOW PROFILE FDA UDI

Identifiers

Primary DI / UDI-DI
00810050862417 FDA UDI
FDA Product Code
BTI FDA UDI
BXO FDA UDI
CAN FDA UDI
GCX FDA UDI
GMDN Term
Laboratory pump, vacuum FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.6250 FDA UDI
868.2900 FDA UDI
868.2700 FDA UDI
880.6740 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

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Non-fixed medical gas cylinder regulatorMedical device air compressorAir/gas pressure transducerLaboratory pump, vacuum

MedPak by Lifeport, Llc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laboratory pump, vacuum.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Lifeport, Llc.

Sources (1)

  • FDA UDI f8dddc3b-cb20-4495-8941-357f8b5ae1ba 34 fields · synced May 31, 2026