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SEIRIN Pyonex Needles

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref PYONEX 1.5mm

by Seirin Corporation

Identity

Trade Name
SEIRIN Pyonex Needles EUDAMED
SEIRIN PYONEX FDA UDI
Generic Name
Acupuncture needle, single-use FDA UDI
Device Name
SEIRIN Pyonex Needles EUDAMED
Designed with both the patient and practitioner in mind, the new and advanced Pyonex™ Singles continue SEIRIN's tradition of gentle, painless and stress free press needles. The patented plastic case and sheath allow the practitioner to insert the needle without touching the needle tip or the surface of the Micropore adhesive tape. This hypoallergenic latex-free adhesive allows the skin to breathe during treatment. With SEIRIN's consistently smooth insertion, the result is a pleasant and painless experience for your patient. FDA UDI
Model / Reference
PYONEX 1.5mm EUDAMED
Pyonex Pink 0.20x1.5mm FDA UDI
Description
Designed with both the patient and practitioner in mind, the new and advanced Pyonex™ Singles continue SEIRIN's tradition of gentle, painless and stress free press needles. The patented plastic case and sheath allow the practitioner to insert the needle without touching the needle tip or the surface of the Micropore adhesive tape. This hypoallergenic latex-free adhesive allows the skin to breathe during treatment. With SEIRIN's consistently smooth insertion, the result is a pleasant and painless experience for your patient. FDA UDI

Identifiers

Primary DI / UDI-DI
04547248420062 EUDAMEDFDA UDI
Basic UDI-DI
4547248SPN001X6 EUDAMED
Unit of Use DI
24547248420066 EUDAMED
FDA Product Code
MQX FDA UDI
EMDN Code
A019002 ACUPUNCTURE NEEDLES EUDAMED
GMDN Term
Acupuncture needle, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
880.5580 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

Yes

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 0.2 Millimeter FDA UDI
Length — 1.5 Millimeter FDA UDI

SEIRIN Pyonex Needles by Seirin Corporation — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Seirin Corporation
EUDAMED SRN
JP-MF-000012274
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED dc191cd3-e509-40de-ab9c-fffa308fe258 61 fields · synced Jul 10, 2026
  • FDA UDI 60d6ccdf-4a2f-4b27-8041-01fe7f693a29 35 fields · synced May 30, 2026