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seca analytics 125

FDA UDI

Class II (US FDA UDI)

by Seca Corp.

Identity

Trade Name
seca analytics 125 FDA UDI
Generic Name
Medical equipment clinical data interfacing software FDA UDI
Device Name
Cloud-based mBCA software for diagnosis and therapy support. FDA UDI
Model / Reference
125 FDA UDI
Description
Cloud-based mBCA software for diagnosis and therapy support. FDA UDI

Identifiers

Catalog Number
1252000012 FDA UDI
Primary DI / UDI-DI
04012030020794 FDA UDI
FDA Product Code
PUH FDA UDI
GMDN Term
Medical equipment clinical data interfacing software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2770 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

seca analytics 125 by Seca Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Seca Corp.

Sources (1)

  • FDA UDI f9360890-b859-47a2-8d07-eaedff338072 36 fields · synced May 30, 2026