Identity
- Trade Name
- FCI NUNCHAKU 90 FDA UDI
- Generic Name
- Lacrimal tube FDA UDI
- Device Name
- FCI NUNCHAKU 90 FDA UDI
- Model / Reference
- S1.1361 FDA UDI
- Description
- FCI NUNCHAKU 90 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 03760087123739 FDA UDI
- FDA Product Code
- OKS FDA UDI
- GMDN Term
- Lacrimal tube FDA UDI
Classification
- Device Class
- U FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Lacrimal tube
Fci Nunchaku 90 by Fci S A S Fci 20 22 — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Lacrimal tube.
- STENTube — QUEST MEDICAL INC · U
- LACRIFLOW CL — Kaneka Corp. · U
- Stradis Medical, LLC. — STRADIS MEDICAL, LLC · Class II
- Rumex — Rumex International Co. · Class II
- Rumex — Rumex International Co. · Class II
- LACRIFLOW — Kaneka Corp. · U
- STRADIS HEALTHCARE — STRADIS MEDICAL, LLC · Class II
- LACRIFLOW — Kaneka Corp. · U
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 U | Pending data |
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Manufacturer
- Manufacturer
- Fci S A S Fci 20 22
Sources (1)
- FDA UDI 237c8774-5045-4c40-9186-a5f2f2bcb9a4 33 fields · synced May 30, 2026