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seca 452

FDA UDI

Class I (US FDA UDI)

by Seca Corp.

Identity

Trade Name
seca 452 FDA UDI
Generic Name
Medical equipment clinical data interfacing software FDA UDI
Device Name
With the Interface Module seca 452 seca scales can be refitted with minimum expense and effort to make them fully integrated via seca software. The module can be installed in a easy-to-assemble holder directly on the product and then configured via the central server. LEDs indicate readiness for use, give the user feedback on the scanned patient barcode and confirm successful transmission of measurements to the electronic medical record system. FDA UDI
Model / Reference
452 FDA UDI
Description
With the Interface Module seca 452 seca scales can be refitted with minimum expense and effort to make them fully integrated via seca software. The module can be installed in a easy-to-assemble holder directly on the product and then configured via the central server. LEDs indicate readiness for use, give the user feedback on the scanned patient barcode and confirm successful transmission of measurements to the electronic medical record system. FDA UDI

Identifiers

Catalog Number
4520050009 FDA UDI
Primary DI / UDI-DI
04012030019644 FDA UDI
FDA Product Code
OUG FDA UDI
GMDN Term
Medical equipment clinical data interfacing software FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6310 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: Medical equipment clinical data interfacing software

seca 452 by Seca Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical equipment clinical data interfacing software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Seca Corp.

Sources (1)

  • FDA UDI 473c5f9c-f3d2-446f-8d1b-213138b74ec6 35 fields · synced May 30, 2026