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Myotech Six Series Dry Needles

FDA UDI

Class II (US FDA UDI)

by Red Coral Acupuncture Supplies Pty Ltd

Identity

Trade Name
Myotech Six Series Dry Needles FDA UDI
Generic Name
Acupuncture needle, single-use FDA UDI
Device Name
Myotech Dry Needles 6 Series 0.30x50mm FDA UDI
Model / Reference
RCMsix3050 FDA UDI
Description
Myotech Dry Needles 6 Series 0.30x50mm FDA UDI

Identifiers

Primary DI / UDI-DI
09351885000212 FDA UDI
510(k) Number
K052731 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

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Acupuncture needle, single-use

Myotech Six Series Dry Needles by Red Coral Acupuncture Supplies Pty Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Acupuncture needle, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 07977b7a-a0a9-4596-8516-10bc53c4b8a7 35 fields · synced May 29, 2026