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Automated sample transfer processing system

EUDAMEDFDA UDI

Class A (EU MDR)

Ref -Model Xpeedy DOA20

by Hangzhou Allsheng Instruments Co., Ltd

Identity

Trade Name
Automated sample transfer processing system EUDAMED
CURA FDA UDI
Generic Name
Pipetting system IVD FDA UDI
Device Name
Automated sample transfer processing system EUDAMED
The Xpeedy DOA20 is used for fluid pre-treatment and processing of samples in a toxicology lab setting, serving the purpose of sample dilution, subpackaging, incubation and sample transferring. FDA UDI
Model / Reference
Xpeedy DOA20 EUDAMEDFDA UDI
- EUDAMED
Description
The Xpeedy DOA20 is used for fluid pre-treatment and processing of samples in a toxicology lab setting, serving the purpose of sample dilution, subpackaging, incubation and sample transferring. FDA UDI

Identifiers

Primary DI / UDI-DI
06975141982086 EUDAMEDFDA UDI
Basic UDI-DI
697514198AS229FL EUDAMED
FDA Product Code
JJH FDA UDI
EMDN Code
W0299 IVD INSTRUMENTS - OTHER EUDAMED
GMDN Term
Pipetting system IVD FDA UDI

Classification

Device Class
Class A EUDAMED
Class I FDA UDI
Regulation Number
862.2310 FDA UDI
Market of Registration
Türkiye EUDAMED
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Automated sample transfer processing system by Hangzhou Allsheng Instruments Co., Ltd — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
CN-MF-000020502
Authorised Representative
RIOMAVIX SOCIEDAD LIMITADA ES-AR-000001202

Sources (2)

  • EUDAMED e7e50e74-01a6-44c0-bc59-93fc49adda4b 61 fields · synced Jun 17, 2026
  • FDA UDI 24b75ac2-0a25-4d69-8da6-b4ef1290497f 34 fields · synced May 30, 2026