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Hm 325

EUDAMEDFDA UDI

Class A (EU MDR)

Ref 902100

by Shandon Diagnostics Limited

Identity

Trade Name
HM 325 EUDAMED
Epredia FDA UDI
Generic Name
Rotary microtome IVD FDA UDI
Device Name
HM325 Rotary Microtome EUDAMED
Model / Reference
902100 EUDAMED
HM325 ROTARY MICROTOME FDA UDI

Identifiers

Primary DI / UDI-DI
05051663010078 EUDAMEDFDA UDI
Basic UDI-DI
5051663SDL017KH EUDAMED
Direct Marketing DI
05051663010078 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

Hm 325 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 9d55d0f0-2e0b-4d28-b4c6-14f8001d5fa8 61 fields · synced Jul 9, 2026
  • FDA UDI 0cd29b49-a419-4e60-8f6e-f75acfe046a2 32 fields · synced May 30, 2026