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Battery

FDA UDI

Class II (US FDA UDI)

by Vitaheat Medical, LLC

Identity

Trade Name
Battery FDA UDI
Generic Name
Primary battery FDA UDI
Device Name
The Model 100026 Battery provides power to the Model 2002 Controller. The Battery is charged by the 3001-C Battery Charger. FDA UDI
Model / Reference
100026 FDA UDI
Description
The Model 100026 Battery provides power to the Model 2002 Controller. The Battery is charged by the 3001-C Battery Charger. FDA UDI

Identifiers

Primary DI / UDI-DI
00851446007036 FDA UDI
510(k) Number
K132454 FDA UDI
FDA Product Code
DWJ FDA UDI
GMDN Term
Primary battery FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5900 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

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

Category: Primary battery

Battery by Vitaheat Medical, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Primary battery.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 02aa36e2-6784-40bc-b42a-5eed9ba557d0 35 fields · synced Jun 8, 2026