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Pulse Oximeter

EUDAMEDFDA UDIFDA 510(k)

Class IIa (EU MDR)

Ref WS20A

by Hunan Accurate Bio-Medical Technology Co., Ltd.

Identity

Trade Name
Pulse Oximeter EUDAMED
Accare® FDA UDI
Generic Name
Pulse oximeter FDA UDI
Device Name
Pulse Oximeter EUDAMED
Model / Reference
WS20A EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
06927394500999 EUDAMEDFDA UDI
Basic UDI-DI
69273945PO03WE EUDAMED
Direct Marketing DI
06927394500999 EUDAMED
FDA Product Code
PGJ FDA UDI
EMDN Code
Z1203020408 PULSE OXIMETERS EUDAMED
GMDN Term
Pulse oximeter FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
870.2700 FDA UDI
Market of Registration
Germany 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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Pulse Oximeter by Hunan Accurate Bio-Medical Technology Co., Ltd. — Class IIa — FDA_510K, MDR — listed in EUDAMED, FDA GUDID, FDA 510(k)

Authorization Coverage (2 countries)

Regulatory Authorizations

United States Active

FDA_510K

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000012835
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (3)

  • EUDAMED bcae3cfc-3e1d-4d56-b83c-47f061cdb55f 61 fields · synced Oct 6, 2026
  • FDA UDI 07de2b53-476e-46b9-af9e-29d868fac22f 32 fields · synced May 29, 2026
  • FDA 510(k) K240808 1 fields · synced May 18, 2026