seca 404 4040000009

GUDID 04012030021593

The ramp is intended to enable the clinical staff to push a patient's wheelchair, bed or stretcher onto the platform of a compatible electronic platform scale.

seca GmbH & Co. KG

Fixed ramp
Primary Device ID04012030021593
NIH Device Record Key1c31a212-4324-4895-a6b7-21003a86b347
Commercial Distribution StatusIn Commercial Distribution
Brand Nameseca 404
Version Model Number404
Catalog Number4040000009
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
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
GS104012030021593 [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 Date2024-05-09
Device Publish Date2024-05-01

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