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seca 232

FDA UDI

Class I (US FDA UDI)

by Seca Corp.

Identity

Trade Name
seca 232 FDA UDI
Generic Name
Infant scale, electronic FDA UDI
Device Name
Analog measuring rod for baby scales seca 333 i. FDA UDI
Model / Reference
232 FDA UDI
Description
Analog measuring rod for baby scales seca 333 i. FDA UDI

Identifiers

Catalog Number
2321817008 FDA UDI
Primary DI / UDI-DI
04012030019439 FDA UDI
FDA Product Code
FRW FDA UDI
GMDN Term
Infant scale, electronic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.2720 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: Infant scale, electronic

seca 232 by Seca Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Infant scale, electronic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Seca Corp.

Sources (1)

  • FDA UDI 7c17f39c-424a-4b11-af6e-cf21fe3567ea 35 fields · synced May 31, 2026