← Back to catalogue

Sp1119

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref 07-10-00Model SP1119

by Shenzhen SINO-K Medical Technology Co., Ltd.

Identity

Trade Name
SP1119 EUDAMED
SINO-K FDA UDI
Generic Name
Pulse oximeter probe, single-use FDA UDI
Device Name
SPO2 Sensor EUDAMED
Disposable SpO2 Sensor FDA UDI
Model / Reference
SP1119 EUDAMEDFDA UDI
07-10-00 EUDAMED
Description
Disposable SpO2 Sensor FDA UDI

Identifiers

Primary DI / UDI-DI
06972820960700 EUDAMEDFDA UDI
Basic UDI-DI
B-06972820960700 EUDAMED
510(k) Number
K192608 FDA UDI
FDA Product Code
DQA FDA UDI
EMDN Code
C900301 PULSE OXIMETER SENSORS EUDAMED
GMDN Term
Pulse oximeter probe, single-use FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
870.2700 FDA UDI
Market of Registration
Ireland 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

Yes

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Pulse oximeter probe, single-use

Sp1119 by Shenzhen SINO-K Medical Technology Co., Ltd. — Class IIb — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pulse oximeter probe, single-use.

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
CN-MF-000021157
Authorised Representative
Prolinx GmbH DE-AR-000005129

Sources (2)

  • EUDAMED 5209f29b-e484-4b76-8c43-beb5be1a31bf 61 fields · synced Jul 15, 2026
  • FDA UDI 96462f78-9211-4b58-b277-050896608003 34 fields · synced May 30, 2026