AccessGUDID - DEVICE: Charder (04719846002258)

GUDID

Device Identifier (DI) Information

Brand Name: Charder
Version or Model: MS6001TB
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: CHARDER ELECTRONIC CO., LTD.

Primary DI Number: 04719846002258
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 656102035 *Terms of Use

Device Description: No description.

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?
35321	Bed scale	A transportable electronic device designed to measure and display the body weight of a patient occupying a bed and who is unable to vacate the bed. It is available in a variety of designs such as a slab-like padded board suspended by metal brackets from a trolley (cart) that contains a weighing mechanism onto which the patient is moved (rolled from the bed onto the slab), or more commonly a system whereby the entire bed (with patient) is weighed and the known weight of the bed and the bedding is subtracted to provide the patient's weight (e.g., pads containing transducers are placed under each wheel or leg of the bed and connected to the electronic weighing 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: 1446c264-5d56-4575-8466-816502af7262
Public Version Date: January 21, 2020
Public Version Number: 1
DI Record Publish Date: January 13, 2020

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
No Package DIs found

Secondary DI

[?]

Issuing Agency [?]	Secondary DI Number
No Secondary DIs found

Unit of Use DI

[?]

Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]

Device Subject to Direct Marking (DM), but Excepted: No
DM DI Different from Primary DI: No
DM DI Number: None
CLOSE

Production Identifier(s) in UDI

[?]

Lot or Batch Number: Yes
Serial Number: No
Expiration Date: No
Manufacturing Date: Yes
Donation Identification Number: Yes CLOSE

Customer Contact

[?]

No Customer Contact currently defined

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