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TDHisto/Cyto

FDA UDI

Class I (US FDA UDI)

by Technidata

Identity

Trade Name
TDHisto/Cyto FDA UDI
Generic Name
Pathology information system application software FDA UDI
Device Name
TDHisto/Cyto is a software used for managing medical information in the field of laboratories performing histology, non-gynecological and gynecological cytology and autopsy activities. . FDA UDI
Model / Reference
TDHisto/Cyto FDA UDI
Description
TDHisto/Cyto is a software used for managing medical information in the field of laboratories performing histology, non-gynecological and gynecological cytology and autopsy activities. . FDA UDI

Identifiers

Primary DI / UDI-DI
03770027519010 FDA UDI
FDA Product Code
JQP FDA UDI
GMDN Term
Pathology information system application software FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2100 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Pathology information system application software

TDHisto/Cyto by Technidata — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pathology information system application software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Technidata

Sources (1)

  • FDA UDI 098b1fde-1161-4743-acda-3dbbfec08cd0 33 fields · synced May 30, 2026