← Back to catalogue

SPO2 Reus Adult Clip Sensor M1196A

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref 989803205901

by Philips Medizin Systeme Böblingen GmbH

Identity

Trade Name
SPO2 Reus Adult Clip Sensor M1196A EUDAMED
SpO2 Sensor FDA UDI
Generic Name
Pulse oximeter probe, reusable FDA UDI
Device Name
SPO2 Sensors EUDAMED
M1196A Reusable Adult SpO2 Clip Sensor (3m) FDA UDI
Model / Reference
989803205901 EUDAMED
SPO2 Reus Adult Clip Sensor M1196A FDA UDI
Description
M1196A Reusable Adult SpO2 Clip Sensor (3m) FDA UDI

Identifiers

Catalog Number
989803205901 FDA UDI
Primary DI / UDI-DI
00884838102569 EUDAMEDFDA UDI
Basic UDI-DI
B-00884838102569 EUDAMED
FDA Product Code
DQA FDA UDI
EMDN Code
Z12030280 VITAL SIGNS MONITORING INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Pulse oximeter probe, reusable FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
870.2700 FDA UDI
Market of Registration
Austria EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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: Electrical-only medical device connection cable, reusable

SPO2 Reus Adult Clip Sensor M1196A by Philips Medizin Systeme Böblingen GmbH — Class IIb — MDD, FDA UDI — listed in EUDAMED, FDA GUDID

Similar devices

Also classified as Electrical-only medical device connection cable, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
DE-MF-000006026

Sources (2)

  • EUDAMED 54ef0351-7155-45d4-ae3e-801c093633a4 61 fields · synced Jun 18, 2026
  • FDA UDI ee1afa71-9509-44d3-9c7f-6b2ba2e4853c 36 fields · synced May 30, 2026