AccessGUDID - DEVICE: Tai Chi™ Power 80 (16970514320103)

GUDID

Device Identifier (DI) Information

Brand Name: Tai Chi™ Power 80
Version or Model: AY7110
Commercial Distribution Status: In Commercial Distribution
Catalog Number: AY7110
Company Name: Suzhou Shenlong Medical Apparatus Co., Ltd.

Primary DI Number: 16970514320103
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 80
Labeler D-U-N-S® Number*: 545745192 *Terms of Use

Device Description: Painless Tai Chi™ needles, in economical bulk packaging. Made of surgical stainless steel, Tai Chi™ Power 80 needles provide practitioners with a high quality needle at an affordable price. The flexible "spring" style metal handle provides superior grip for the practitioner, while the advanced manufacturing process provides a painless experience for the patient. Each easy-open plastic package contains eight sterile acupuncture needles with one insertion tube. Box of 80 needles, 0.25 x 40 mm.

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 [?]
K023787	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
Device Size Text, specify: 0.25 x 40 mm

Device Record Status

Public Device Record Key: 1e11a424-671d-4165-a870-2c805168e102
Public Version Date: July 06, 2018
Public Version Number: 3
DI Record Publish Date: July 22, 2016