Identity
- Trade Name
- HM 325 EUDAMEDEpredia FDA UDI
- Generic Name
- Rotary microtome IVD FDA UDI
- Device Name
- HM325 Rotary Microtome EUDAMEDRotary Microtome FDA UDI
- Model / Reference
- 902100-UK EUDAMEDHM 325 Rotary Microtome (UK made) FDA UDI
- Description
- Rotary Microtome FDA UDI
Identifiers
- Catalog Number
- 902100-UK FDA UDI
- Primary DI / UDI-DI
- 05051663010528 EUDAMEDFDA UDI
- Basic UDI-DI
- 5051663SDL017KH EUDAMED
- Direct Marketing DI
- 05051663010528 EUDAMED
- FDA Product Code
- IDO FDA UDI
- EMDN Code
- W0202059005 MICROTOMES EUDAMED
- GMDN Term
- Rotary microtome IVD FDA UDI
Classification
- Device Class
- Class A EUDAMEDClass 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 5051663SDL017KH | Class A | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class A | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Shandon Diagnostics Limited
- EUDAMED SRN
- GB-MF-000008187
- Authorised Representative
- Epredia Netherlands B.V. NL-AR-000001488
Sources (2)
- EUDAMED e4899eaa-d3ab-4a51-82a1-3d7b1820ec9a 61 fields · synced Jul 17, 2026
- FDA UDI 03108602-23c1-42a8-b8cc-4e6046495319 34 fields · synced May 30, 2026