AccessGUDID - DEVICE: seca 496 (04012030021494)

GUDID

Device Identifier (DI) Information

Brand Name: seca 496
Version or Model: 496
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 4960000009
Company Name: seca GmbH & Co. KG

Primary DI Number: 04012030021494
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 316584937 *Terms of Use

Device Description: The display is intended to operate a compatible electronic platform scale. The interface box enables the power supply and the display to be connected to a compatible electronic platform scale. seca 496 can also be connected to an external device for the transmission of measurement data. The display seca 496 must be combined with a compatible electronic platform scale to enable the measurement of weight.

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	No
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
36615	Image display unit, monochrome	An electrically-powered visual display unit (VDU), commonly known as a screen or a monitor [e.g., cathode-ray tube (CRT) or liquid crystal display (LCD)], designed for displaying graphical information (e.g., values or images measured/acquired by other devices) in only one colour. The device(s) that generates the visual data is not included with the display unit.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FRW	SCALE, PATIENT

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 8ca912c8-b854-4907-a25a-9af16c470db4
Public Version Date: May 09, 2024
Public Version Number: 1
DI Record Publish Date: May 01, 2024