AcuTek Copper Bulk Acupuncture Needle

GUDID 00831592004998

The AcuTek Copper Handle Bulk Acupuncture Needle is well known for its smooth and painless insertion. It is one of the best acupuncture needles in the U.S.

UPC MEDICAL SUPPLIES, INC.

Acupuncture needle, single-use

Primary Device ID	00831592004998
NIH Device Record Key	53085eda-0104-4008-8ca4-19b8465b552f
Commercial Distribution Discontinuation	2020-05-30
Commercial Distribution Status	In Commercial Distribution
Brand Name	AcuTek Copper Bulk Acupuncture Needle
Version Model Number	A-2C 0.20 X 25mm
Company DUNS	942011719
Company Name	UPC MEDICAL SUPPLIES, INC.
Device Count	500
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Device Dimensions

Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter
Length	25 Millimeter
Outer Diameter	0.2 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00008315920000 [Unit of Use]
GS1	00831592004998 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K974122

FDA Product Code

MQX	Needle, Acupuncture, Single Use

Sterilization

Steralize Prior To Use	false
Device Is Sterile	true

Device Entry Metadata

Public Version Status	Update
Device Record Status	Published
Public Version Number	3
Public Version Date	2018-07-06
Device Publish Date	2017-05-31

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