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HemoFlow 500 XS

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 905000002

by Applied Science, Inc.

Identity

Trade Name
HemoFlow 500 XS EUDAMED
HemoFlow FDA UDI
Generic Name
Blood donation rocker FDA UDI
Device Name
HemoFlow 500 XS EUDAMED
HemoFlow 500 XS/Blood Donation Rocker FDA UDI
Model / Reference
905000002 EUDAMED
9-0500-0002 FDA UDI
Description
HemoFlow 500 XS/Blood Donation Rocker FDA UDI

Identifiers

Primary DI / UDI-DI
00850047037077 EUDAMEDFDA UDI
Basic UDI-DI
08500470379050000022X EUDAMED
Direct Marketing DI
00850047037077 EUDAMED
FDA Product Code
KSQ FDA UDI
EMDN Code
W02070103,W02070404 EUDAMED
GMDN Term
Blood donation rocker FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
864.9195 FDA UDI
Market of Registration
Northern Ireland 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

HemoFlow 500 XS by Applied Science, Inc. — 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

EUDAMED SRN
US-MF-000040843
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED ff990eed-77e3-4fd1-8a36-679e236bb21f 61 fields · synced Jun 20, 2026
  • FDA UDI 49cdcff3-a4ae-40e5-a172-54ce51649975 35 fields · synced May 29, 2026