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 ID: 04012030008952
• NIH Device Record Key: 468bc389-95ee-473d-92c5-d8a6d3831a60
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: seca 213
• Version Model Number: 213
• Catalog Number: 2131821009
• Company DUNS: 316584937
• Company Name: seca GmbH & Co. KG
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)5427322
• Email: info.us@seca.com
• Phone: +1(800)5427322
• Email: info.us@seca.com
• Phone: +1(800)5427322
• Email: info.us@seca.com
• Phone: +1(800)5427322
• Email: info.us@seca.com
• Phone: +1(800)5427322
• Email: info.us@seca.com
• Phone: +1(800)5427322
• Email: info.us@seca.com
• Phone: +1(800)5427322
• Email: info.us@seca.com
• Phone: +1(800)5427322
• Email: info.us@seca.com
• Phone: +1(800)5427322
• Email: info.us@seca.com
• Phone: +1(800)5427322
• Email: info.us@seca.com
• Phone: +1(800)5427322
• Email: info.us@seca.com
• Phone: +1(800)5427322
• Email: info.us@seca.com
• Phone: +1(800)5427322
• Email: info.us@seca.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04012030008952 [Primary]

FDA Product Code

• FRW: SCALE, PATIENT

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-09-08
• Device Publish Date: 2020-08-31

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