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ANNE Limb Sensor

FDA UDI

Class II (US FDA UDI)

by Sibel Health Inc.

Identity

Trade Name
ANNE Limb Sensor FDA UDI
Generic Name
Wearable multiple physiological parameter recorder, reusable FDA UDI
Model / Reference
810-00013 FDA UDI

Identifiers

Primary DI / UDI-DI
00850064210156 FDA UDI
510(k) Number
K240305 FDA UDI
FDA Product Code
DQA FDA UDI
DRG FDA UDI
FLL FDA UDI
GMDN Term
Wearable multiple physiological parameter recorder, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2700 FDA UDI
870.2910 FDA UDI
880.2910 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Pulse oximeterWearable multiple physiological parameter recorder, reusable

ANNE Limb Sensor by Sibel Health 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

Manufacturer
Sibel Health Inc.

Sources (1)

  • FDA UDI 919bd494-ce4c-45f0-984b-be2cfefc6f09 33 fields · synced May 30, 2026