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Vave

FDA UDI

Class II (US FDA UDI)

by Vave Health Inc

Identity

Trade Name
Vave FDA UDI
Generic Name
Portable/mobile rechargeable battery pack FDA UDI
Device Name
Removable Lithium Ion Battery FDA UDI
Model / Reference
VBT FDA UDI
Description
Removable Lithium Ion Battery FDA UDI

Identifiers

Catalog Number
VBT FDA UDI
Primary DI / UDI-DI
00850001977012 FDA UDI
510(k) Number
K191541 FDA UDI
FDA Product Code
ITX FDA UDI
IYO FDA UDI
GMDN Term
Portable/mobile rechargeable battery pack FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1570 FDA UDI
892.1560 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: Portable/mobile rechargeable battery pack

Vave by Vave Health Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Portable/mobile rechargeable battery pack.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vave Health Inc

Sources (1)

  • FDA UDI 6ae5afc1-38ce-403b-8e77-a64e63b14a49 37 fields · synced May 30, 2026