seca 417 4171821009

GUDID 04012030008907

Light and stable measuring board for mobile use.

seca GmbH & Co. KG

Patient-height measure
Primary Device ID04012030008907
NIH Device Record Key9995c1cb-facd-4233-964e-853bd5b28d76
Commercial Distribution StatusIn Commercial Distribution
Brand Nameseca 417
Version Model Number417
Catalog Number4171821009
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
GS104012030008907 [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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