← Back to catalogue

Thermo Fisher

FDA UDI

Class I (US FDA UDI)

by Shandon Diagnostics Limited

Identity

Trade Name
Thermo Fisher FDA UDI
Generic Name
Tissue processor IVD, automated/semi-automated FDA UDI
Device Name
100-240V 50/60Hz (CHINA ONLY) FDA UDI
Model / Reference
Excelsior AS FDA UDI
Description
100-240V 50/60Hz (CHINA ONLY) FDA UDI

Identifiers

Primary DI / UDI-DI
05051663003001 FDA UDI
FDA Product Code
IEO FDA UDI
GMDN Term
Tissue processor IVD, automated/semi-automated FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3875 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Category: Tissue processor IVD, automated/semi-automated

Thermo Fisher by Shandon Diagnostics Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tissue processor IVD, automated/semi-automated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 0cb2baa0-104a-4d25-a00b-327fb7d6e9cf 33 fields · synced May 30, 2026