seca 453 4530000004

GUDID 04012030021449

The intended use of this product, resulting from the combination of the medical devices: - scale: seca 654, seca 655 - handrail: seca 455 - battery pack: seca 453 is to power the handrail scale during the mobile use, so that the clinical staff has not to plug in the power adapter into an AC outlet when patients are measured in their patient room, while the scale is used for conventional determination of weight.

seca GmbH & Co. KG

Portable/mobile rechargeable battery pack

• Primary Device ID: 04012030021449
• NIH Device Record Key: 8e01b829-6563-4e98-aba5-3aaa81f22094
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: seca 453
• Version Model Number: 453
• Catalog Number: 4530000004
• 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	04012030021449 [Primary]

FDA Product Code

• FRI: SCALE, STAND-ON, 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: 2023-11-09
• Device Publish Date: 2023-11-01

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