Identity
- Trade Name
- ACHILLON® FDA UDI
- Generic Name
- Wire/ligature passer, reusable FDA UDI
- Device Name
- Minimally invasive Achilles tendon suture system Achillon® FDA UDI
- Model / Reference
- 119700ND FDA UDI
- Description
- Minimally invasive Achilles tendon suture system Achillon® FDA UDI
Identifiers
- Catalog Number
- 119 700 FDA UDI
- Primary DI / UDI-DI
- 10381780043294 FDA UDI
- FDA Product Code
- HCF FDA UDI
- GMDN Term
- Wire/ligature passer, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
Category: Wire/ligature passer, reusable
Achillon® by Newdeal Sas — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Newdeal Sas
Sources (1)
- FDA UDI 39a8f091-a409-4f43-91b5-a9a2d9f233f5 37 fields · synced Jun 8, 2026