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seca 210

FDA UDI

Class I (US FDA UDI)

by Seca Corp.

Identity

Trade Name
seca 210 FDA UDI
Generic Name
Patient-height measure FDA UDI
Device Name
The seca 210 measuring mat is designed for use in paediatric practices, paediatric hospitals or for home visits by midwives and paediatricians. The measuring mat can be rolled up and so requires only a little space. There are also holes in the head stop on the mat to enable it to be hung on a wall. FDA UDI
Model / Reference
210 FDA UDI
Description
The seca 210 measuring mat is designed for use in paediatric practices, paediatric hospitals or for home visits by midwives and paediatricians. The measuring mat can be rolled up and so requires only a little space. There are also holes in the head stop on the mat to enable it to be hung on a wall. FDA UDI

Identifiers

Catalog Number
2101721004 FDA UDI
Primary DI / UDI-DI
04012030014304 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Patient-height measure

seca 210 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 19ec273a-9072-4373-b1ab-5c50129012cb 35 fields · synced May 30, 2026