MedPak

FDA UDI

Class I (US FDA UDI)

by Lifeport, Llc.

Identity

Trade Name: MedPak FDA UDI
Generic Name: Air/gas pressure transducer FDA UDI
Device Name: ASSEMBLY – MEDPAK FDA UDI
Model / Reference: MP2-001-05 FDA UDI
Description: ASSEMBLY – MEDPAK FDA UDI

Identifiers

Primary DI / UDI-DI: 00810050861687 FDA UDI
FDA Product Code: BXO FDA UDI
CAN FDA UDI
GCX FDA UDI
GMDN Term: Air/gas pressure transducer FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 868.2900 FDA UDI
868.2700 FDA UDI
880.6740 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Non-fixed medical gas cylinder regulator Medical device air compressor Air/gas pressure transducer

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

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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 I	Pending data

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Manufacturer

Manufacturer: Lifeport, Llc.

Sources (1)

FDA UDI 9a11a8e0-7159-4f94-81d4-a63b48ad2049 34 fields · synced Jun 1, 2026