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Ligature Director YS-704A Twister

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 22754Model ORTHODONTIC LIGATURE INSTRUMENTS

by Ydm Corporation

Identity

Trade Name
Ligature Director YS-704A Twister EUDAMED
NA FDA UDI
Generic Name
Orthodontic ligature director FDA UDI
Device Name
Ligature Director EUDAMED
Used to tuck and direct ligatures under the archwire or bracket wings or to push archwires or auxiliaries into position, also to ligate wires. FDA UDI
Model / Reference
ORTHODONTIC LIGATURE INSTRUMENTS EUDAMED
22754 EUDAMEDFDA UDI
Description
Used to tuck and direct ligatures under the archwire or bracket wings or to push archwires or auxiliaries into position, also to ligate wires. FDA UDI

Identifiers

Catalog Number
22754 FDA UDI
Primary DI / UDI-DI
04963931227549 EUDAMEDFDA UDI
Basic UDI-DI
4963931YDM00003WJ EUDAMED
FDA Product Code
ECP FDA UDI
EMDN Code
L150701 ORTHODONTIC LIGATURE TOOLS, REUSABLE EUDAMED
GMDN Term
Orthodontic ligature director FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.4565 FDA UDI
Market of Registration
Spain EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Ligature Director YS-704A Twister by Ydm Corporation — Class I — 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
Ydm Corporation
EUDAMED SRN
JP-MF-000011653
Authorised Representative
MedEnvoy Global BV NL-AR-000024028

Sources (2)

  • EUDAMED a555dc81-9c89-4e12-989f-1ce47e4b700c 61 fields · synced Aug 4, 2026
  • FDA UDI e557412a-0460-49fb-8cb2-2fa7c8e134ed 35 fields · synced May 30, 2026