Tai Chi 7 Star Dermal Needle

FDA UDI

Class II (US FDA UDI)

by Suzhou Shenlong Medical Apparatus Co., Ltd.

Identity

Trade Name: Tai Chi 7 Star Dermal Needle FDA UDI
Generic Name: Acupuncture needle, single-use FDA UDI
Device Name: Painless Tai Chi™ needles, in blister packaging. Made of surgical stainless steel, Tai Chi™ needles provide practitioners with a high quality needle at an affordable price. The flexible plastic 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 one acupuncture needle. Box of 1 needle, 0.45, 0.75 x 3 mm. FDA UDI
Model / Reference: BY2623 FDA UDI
Description: Painless Tai Chi™ needles, in blister packaging. Made of surgical stainless steel, Tai Chi™ needles provide practitioners with a high quality needle at an affordable price. The flexible plastic 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 one acupuncture needle. Box of 1 needle, 0.45, 0.75 x 3 mm. FDA UDI

Identifiers

Catalog Number: BY2623 FDA UDI
Primary DI / UDI-DI: 16970514320653 FDA UDI
510(k) Number: K023787 FDA UDI
FDA Product Code: MQX FDA UDI
GMDN Term: Acupuncture needle, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5580 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Acupuncture needle, single-use

Tai Chi 7 Star Dermal Needle by Suzhou Shenlong Medical Apparatus Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Suzhou Shenlong Medical Apparatus Co., Ltd.

Sources (1)

FDA UDI b0b4043e-d451-46d6-8e0e-ae41b325cc6b 37 fields · synced May 30, 2026

Tai Chi 7 Star Dermal Needle

Identity

Identifiers

Classification

Clinical & Handling

Similar devices

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

Manufacturer

Sources (1)