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Ligature Director YS-704B Double End
EUDAMEDFDA UDIClass I (EU MDR)
Ref 22755Model ORTHODONTIC LIGATURE INSTRUMENTS
Identity
- Trade Name
- Ligature Director YS-704B Double End EUDAMEDNA FDA UDI
- Generic Name
- Orthodontic ligature director FDA UDI
- Device Name
- Ligature Director EUDAMEDUsed 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 EUDAMED22755 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
- 22755 FDA UDI
- Primary DI / UDI-DI
- 04963931227556 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
Moist Heat or Steam Sterilization FDA UDI
Ligature Director YS-704B Double End 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 4963931YDM00003WJ | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Ydm Corporation
- EUDAMED SRN
- JP-MF-000011653
- Authorised Representative
- MedEnvoy Global BV NL-AR-000024028
Sources (2)
- EUDAMED 48351151-45c6-4035-9c3c-699c6d1c204a 61 fields · synced Jul 17, 2026
- FDA UDI 5c608c25-4abf-4569-8eda-997b2734b7d8 35 fields · synced May 30, 2026