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BabySat 3 Rx Base Station

FDA UDI

Class II (US FDA UDI)

by Owlet Baby Care, Inc.

Identity

Trade Name
BabySat 3 Rx Base Station FDA UDI
Generic Name
Multiple vital physiological parameter monitoring system, home-use FDA UDI
Model / Reference
OBL 3.0-M1 FDA UDI

Identifiers

Primary DI / UDI-DI
00810099090024 FDA UDI
510(k) Number
K222597 FDA UDI
FDA Product Code
DQA FDA UDI
GMDN Term
Multiple vital physiological parameter monitoring system, home-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2700 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: Multiple vital physiological parameter monitoring system, home-use

BabySat 3 Rx Base Station by Owlet Baby Care, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple vital physiological parameter monitoring system, home-use.

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 fdeeb52c-a578-4939-afeb-fd106e87cdf6 33 fields · synced May 30, 2026