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Adult SpO2 Grips (20)

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 989803166551

by Philips Medizin Systeme Böblingen GmbH

Identity

Trade Name
Adult SpO2 Grips (20) EUDAMED
MR Patient Care Adult SpO2 Grips (20) FDA UDI
Generic Name
Pulse oximeter probe, single-use FDA UDI
Device Name
Reusable SpO2 Clips and Single use Grips EUDAMED
Box of 20 Disposable SpO2 finger grips designed for use with the Quick Connect SPO2 Sensor (989803161991) - Sized for Adult patients FDA UDI
Model / Reference
989803166551 EUDAMED
Adult SpO2 Grips (20) FDA UDI
Description
Box of 20 Disposable SpO2 finger grips designed for use with the Quick Connect SPO2 Sensor (989803161991) - Sized for Adult patients FDA UDI

Identifiers

Catalog Number
989803166551 FDA UDI
Primary DI / UDI-DI
10884838117881 EUDAMEDFDA UDI
Basic UDI-DI
0884838BM1070LW EUDAMED
FDA Product Code
MWI FDA UDI
EMDN Code
Z1203020299 MULTI–PARAMETER MONITORS - OTHER EUDAMED
GMDN Term
Pulse oximeter probe, single-use FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
870.2300 FDA UDI
Market of Registration
Austria EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Adult SpO2 Grips (20) by Philips Medizin Systeme Böblingen GmbH — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Philips Medizin Systeme Böblingen GmbH
EUDAMED SRN
DE-MF-000006026

Sources (2)

  • EUDAMED 46987a90-b215-4590-8745-ee3881afe4bf 61 fields · synced Jun 18, 2026
  • FDA UDI 54a2b3ef-1787-48cf-bf63-b1733880c2b3 35 fields · synced May 30, 2026