seca 446 4465100009

GUDID 04012030021609

The guardrail is intended to prevent the clinical staff from accidentally pushing a patient's wheelchair, stretcher or bed over the side edge of a compatible scale to enable a safe weighing of patients sitting in a wheelchair or lying in a bed or on a stretcher.

seca GmbH & Co. KG

Wheelchair-accessible platform scale

• Primary Device ID: 04012030021609
• NIH Device Record Key: 62885bab-fe9b-464b-841e-aa2b13217b24
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: seca 446
• Version Model Number: 446
• Catalog Number: 4465100009
• 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
• 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	04012030021609 [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: 2024-05-09
• Device Publish Date: 2024-05-01

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