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BioButton At-Home Kit

FDA UDI

Class II (US FDA UDI)

by Biointellisense, Inc.

Identity

Trade Name
BioButton At-Home Kit FDA UDI
Generic Name
Wearable multiple physiological parameter recorder, reusable FDA UDI
Device Name
BioButton At-Home Kit FDA UDI
Model / Reference
KIT-BBR-3763-2 FDA UDI
Description
BioButton At-Home Kit FDA UDI

Identifiers

Primary DI / UDI-DI
00850005949381 FDA UDI
510(k) Number
K212957 FDA UDI
FDA Product Code
DRG FDA UDI
GMDN Term
Wearable multiple physiological parameter recorder, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2910 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Wearable multiple physiological parameter recorder, reusable

BioButton At-Home Kit by Biointellisense, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wearable multiple physiological parameter recorder, reusable.

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 aa3339e6-aa2e-4f51-a968-1458e1512145 34 fields · synced Jun 8, 2026