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seca 212

FDA UDI

Class I (US FDA UDI)

by Seca Corp.

Identity

Trade Name
seca 212 FDA UDI
Generic Name
Patient-height measure FDA UDI
Device Name
The seca 212 is a portable measuring tape for measuring the head circumference of infants and toddlers. It is made of non-stretch material for use in paediatric care. FDA UDI
Model / Reference
212 FDA UDI
Description
The seca 212 is a portable measuring tape for measuring the head circumference of infants and toddlers. It is made of non-stretch material for use in paediatric care. FDA UDI

Identifiers

Catalog Number
2121817009 FDA UDI
Primary DI / UDI-DI
04012030003759 FDA UDI
FDA Product Code
FRW FDA UDI
GMDN Term
Patient-height measure 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Patient-height measure

seca 212 by Seca Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient-height measure.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Seca Corp.

Sources (1)

  • FDA UDI e8b5ad6d-5732-43e9-81e2-c4a48deceb00 35 fields · synced May 30, 2026