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88001298

EUDAMEDFDA UDIFDA 510(k)

Class IIa (EU MDR)

Ref 88001298Model uOmnispace.MIRef 88002686Model uOmnispace.MR

by Shanghai United Imaging Healthcare Co., Ltd.

Identity

Trade Name
uOmnispace EUDAMEDFDA UDI
Generic Name
Radiology DICOM image processing application software FDA UDI
Device Name
Medical Image Post-processing Software FDA UDI
Model / Reference
uOmnispace.MI EUDAMEDFDA UDI
88001298 EUDAMED
uOmnispace.MR EUDAMED
88002686 EUDAMED
Description
Medical Image Post-processing Software FDA UDI

Identifiers

Primary DI / UDI-DI
06971576834242 EUDAMEDFDA UDI
06971576834372 EUDAMED
Basic UDI-DI
697157683424NN EUDAMED
697157683425NQ EUDAMED
510(k) Number
K233176 FDA UDI
FDA Product Code
LLZ FDA UDI
EMDN Code
Z11020392 INTEGRATED CT/PET SYSTEMS - MEDICAL DEVICE SOFTWARE EUDAMED
Z11050192 MAGNETIC RESONANCE (MR) SYSTEMS - MEDICAL DEVICE SOFTWARE EUDAMED
GMDN Term
Radiology DICOM image processing application software FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
892.2050 FDA UDI
Special Device Type
Software EUDAMED
Market of Registration
Poland EUDAMED
Italy 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

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

88001298 by Shanghai United Imaging Healthcare Co., Ltd. — Class IIa — FDA_510K, MDR — listed in EUDAMED, FDA GUDID, FDA 510(k) — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

United States Active

FDA_510K

United States Active

FDA_510K

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000008501
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (4)

  • EUDAMED ec379fd9-61cf-4b03-80e2-7ac5dc678dc9 61 fields · synced Oct 6, 2026
  • FDA UDI 8c89d5b3-2e41-4281-ab83-583d313ac86c 35 fields · synced May 30, 2026
  • EUDAMED a8dbaf2e-895c-474f-ab81-072771cff194 61 fields · synced Jul 18, 2026
  • FDA 510(k) K230039 1 fields · synced May 18, 2026