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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
LIFE2000 COMPRESSOR FILTER PAC FDA UDI
Model / Reference
BT-80-0005 FDA UDI
Description
LIFE2000 COMPRESSOR FILTER PAC FDA UDI

Identifiers

Primary DI / UDI-DI
00887761979048 FDA UDI
FDA Product Code
BTI FDA UDI
GMDN Term
Medical device air compressor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.6250 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe 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

Similar devices

Also classified as Medical device air compressor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2338e390-9428-4362-8092-b736fde68a92 34 fields · synced May 30, 2026