Life2000

FDA UDI

Class II (US FDA UDI)

by Hill-Rom Services Pte. Ltd.

Identity

Trade Name: Life2000 FDA UDI
Generic Name: Medical device air compressor FDA UDI
Device Name: BREATHE LIFE2000 VENTILATOR PACKAGE HOSPITAL FDA UDI
Model / Reference: BT-20-0007 FDA UDI
Description: BREATHE LIFE2000 VENTILATOR PACKAGE HOSPITAL FDA UDI

Identifiers

Primary DI / UDI-DI: 00887761978195 FDA UDI
FDA Product Code: CBK FDA UDI
GMDN Term: Medical device air compressor FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.5895 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

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Medical device air compressor

Life2000 by Hill-Rom Services Pte. Ltd. — Class II — 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 II	Pending data

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Manufacturer

Manufacturer: Hill-Rom Services Pte. Ltd.

Sources (1)

FDA UDI bd7be61d-d355-41fc-a2a7-9bc55ebcb5d5 34 fields · synced May 30, 2026