AccessGUDID - DEVICE: Economy Plastic Cups #5 (28800018914643)

GUDID

Device Identifier (DI) Information

Brand Name: Economy Plastic Cups #5
Version or Model: DB 310-5
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: Dong Bang Medical co.,Ltd.

Primary DI Number: 28800018914643
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 689846367 *Terms of Use

Device Description: 1000 units in single package

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?
45167	Moxa	A product of the mugwort plant (Artemisia vulgaris) used in traditional Chinese medicine for moxibustion therapy, the slow combustion of moxa as a heat treatment on acupuncture/meridian points. The device is typically applied directly to the skin (with or without adhesive), or placed in a specialized container that is applied to the skin, or onto acupuncture needle handles to heat the needle. The device is supplied in various forms (e.g., in rolls, with adhesive backing, or as loose fibres/threads). This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
KNM	Device, Pressure Applying

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: 4c314c72-7f71-4e20-ae5e-33bdf069dc5d
Public Version Date: January 23, 2023
Public Version Number: 1
DI Record Publish Date: January 15, 2023

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: No CLOSE

Customer Contact

[?]

No Customer Contact currently defined

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