seca 216 2161814009

GUDID 04012030005883

The seca 216 has a variable scale with a range of 3.5 to 230 centimeters that is inserted into a 138 cm frame. The plastic frame is simply mounted on the wall at the desired height. As the user can choose the range shown in the frame, the seca 216 is suitable for measuring children or adults. The results are clearly displayed in a window on the side of the rod and held in place by the locking screw on the head piece. Suitable for international use, the scale is printed in centimeters on one side of the tape and centimeters and inches on the other.

seca GmbH & Co. KG

Patient-height measure
Primary Device ID04012030005883
NIH Device Record Keya71d1e60-a703-4d96-b00e-5934ba8ca27b
Commercial Distribution StatusIn Commercial Distribution
Brand Nameseca 216
Version Model Number216
Catalog Number2161814009
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
GS104012030005883 [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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