AccessGUDID - DEVICE: STERILE ACUPUNCTURE NEEDLES FOR SINGLE USE (06971685273758)

GUDID

Device Identifier (DI) Information

Brand Name: STERILE ACUPUNCTURE NEEDLES FOR SINGLE USE
Version or Model: 0.25*15
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: Changchun AIK Medical Devices Co., Ltd.

Primary DI Number: 06971685273758
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 500
Labeler D-U-N-S® Number*: 543439762 *Terms of Use

Device Description: The AIK Sterile Acupuncture Needles are manufactured from stainless steel and sterilized with ethylene oxide gas. Ten needles with one tube per sterile, individually packed a pouch, 500 needles per box.

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:	Yes
Prescription Use (Rx):	Yes
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?
34175	Acupuncture needle, single-use	A sterile, long, slender, sharply-pointed instrument used to stimulate peripheral nerves in order to produce surgical anaesthesia, relieve pain, and to promote other therapeutic effects. It is widely used in complementary therapy. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
MQX	Needle, Acupuncture, Single Use

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K162566	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
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: a4c71367-7b72-44f2-aff3-c642c958f5b7
Public Version Date: October 08, 2019
Public Version Number: 1
DI Record Publish Date: September 30, 2019