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Hm340e

EUDAMEDFDA UDI

Class A (EU MDR)

Ref 905190-UK

by Shandon Diagnostics Limited

Identity

Trade Name
HM340E EUDAMED
Epredia FDA UDI
Generic Name
Rotary microtome IVD FDA UDI
Device Name
HM340E Rotary Microtome EUDAMED
Rotary Microtome FDA UDI
Model / Reference
905190-UK EUDAMED
HM 340E Rotary Microtome (UK made) FDA UDI
Description
Rotary Microtome FDA UDI

Identifiers

Catalog Number
905190-UK FDA UDI
Primary DI / UDI-DI
05051663010559 EUDAMEDFDA UDI
Basic UDI-DI
5051663SDL018KK EUDAMED
Direct Marketing DI
05051663010559 EUDAMED
FDA Product Code
IDO FDA UDI
EMDN Code
W0202059005 MICROTOMES EUDAMED
GMDN Term
Rotary microtome IVD FDA UDI

Classification

Device Class
Class A EUDAMED
Class I FDA UDI
Regulation Number
864.3010 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
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

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

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

Hm340e by Shandon Diagnostics Limited — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
GB-MF-000008187
Authorised Representative
Epredia Netherlands B.V. NL-AR-000001488

Sources (2)

  • EUDAMED 3fdccae8-4970-4f42-b16b-b403d7ecd886 61 fields · synced Jun 19, 2026
  • FDA UDI 6c9a1e52-ece2-4074-8f52-de122fe5516d 34 fields · synced May 30, 2026