seca 213 2131821009

GUDID 04012030008952

At only 2.4 kg, the seca 213 mobile stadiometer is especially suitable for use in the field but also ideal for doctors’ practices and pediatric hospitals. The measuring rod can be dismantled into several pieces and set up easily and quickly. The spacer keeps the rod straight and stable without any fittings. As the scale is printed along the side of the measuring rod, it is easy to read off the result while measuring, thus guaranteeing precise results.

seca GmbH & Co. KG

Patient-height measure
Primary Device ID04012030008952
NIH Device Record Key468bc389-95ee-473d-92c5-d8a6d3831a60
Commercial Distribution StatusIn Commercial Distribution
Brand Nameseca 213
Version Model Number213
Catalog Number2131821009
Company DUNS316584937
Company Nameseca GmbH & Co. KG
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)5427322
Emailinfo.us@seca.com
Phone+1(800)5427322
Emailinfo.us@seca.com
Phone+1(800)5427322
Emailinfo.us@seca.com
Phone+1(800)5427322
Emailinfo.us@seca.com
Phone+1(800)5427322
Emailinfo.us@seca.com
Phone+1(800)5427322
Emailinfo.us@seca.com
Phone+1(800)5427322
Emailinfo.us@seca.com
Phone+1(800)5427322
Emailinfo.us@seca.com
Phone+1(800)5427322
Emailinfo.us@seca.com
Phone+1(800)5427322
Emailinfo.us@seca.com
Phone+1(800)5427322
Emailinfo.us@seca.com
Phone+1(800)5427322
Emailinfo.us@seca.com
Phone+1(800)5427322
Emailinfo.us@seca.com

Device Identifiers

Device Issuing AgencyDevice ID
GS104012030008952 [Primary]

FDA Product Code

FRWSCALE, PATIENT

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-09-08
Device Publish Date2020-08-31

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