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Buddy Lite, Battery Housing And Heater Unit, Switzerland

FDA UDI

Class II (US FDA UDI)

by Belmont Instrument Corp.

Identity

Trade Name
BUDDY LITE, BATTERY HOUSING AND HEATER UNIT, SWITZERLAND FDA UDI
Generic Name
Conduction blood/fluid warmer FDA UDI
Device Name
BUDDY LITE, BATTERY HOUSING AND HEATER UNIT, SWITZERLAND, CHARGER FDA UDI
Model / Reference
905-00019 FDA UDI
Description
BUDDY LITE, BATTERY HOUSING AND HEATER UNIT, SWITZERLAND, CHARGER FDA UDI

Identifiers

Primary DI / UDI-DI
40896128002495 FDA UDI
510(k) Number
K090508 FDA UDI
FDA Product Code
BSB FDA UDI
GMDN Term
Conduction blood/fluid warmer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.9205 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Buddy Lite, Battery Housing And Heater Unit, Switzerland by Belmont Instrument Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K090508 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Belmont Instrument Corp.

Sources (1)

  • FDA UDI 0ce766cc-d327-4b9e-bd73-3bf7f3f78899 35 fields · synced Jun 1, 2026