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Movano Health

FDA UDI

Class II (US FDA UDI)

by Movano Inc.

Identity

Trade Name
Movano Health FDA UDI
Generic Name
Pulse oximeter FDA UDI
Device Name
EvieMED Ring Kit FDA UDI
Model / Reference
EvieMED Ring, Size 9, Silver FDA UDI
Description
EvieMED Ring Kit FDA UDI

Identifiers

Catalog Number
EvieMEDKit-9-SFP FDA UDI
Primary DI / UDI-DI
00850047602312 FDA UDI
510(k) Number
K241090 FDA UDI
FDA Product Code
DQA FDA UDI
GMDN Term
Pulse oximeter 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

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Pulse oximeter

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

Similar devices

Also classified as Pulse oximeter.

Cleared under the same submission

K241090 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Movano Inc.

Sources (1)

  • FDA UDI 9d9e5ead-5393-48de-b743-8a66a4d3295c 35 fields · synced Jun 8, 2026