Identity
- Trade Name
- LACRIJET® 45 FDA UDI
- Generic Name
- Lacrimal intubation set FDA UDI
- Device Name
- A collection of devices intended to be used to maintain patency of the nasolacrimal system typically for treating/preventing pathologies of the tear drainage system (e.g., post-chemotherapy stenosis) or after dacryocystorhinostomy (DCR). It consists of a long and flexible bicanalicular or monocanalicular tube (e.g., Crawford type) inserted through the lacrimal puncta into the canaliculi, lacrimal sac, and/or nasolacrimal duct; devices to assist the intubation procedure are typically provided preassembled to the tube (e.g., cannula, probes, bougies, introducer, stylet). The tube is typically left in place long-term before removal. This is a single-use device. FDA UDI
- Model / Reference
- S1.1545 FDA UDI
- Description
- A collection of devices intended to be used to maintain patency of the nasolacrimal system typically for treating/preventing pathologies of the tear drainage system (e.g., post-chemotherapy stenosis) or after dacryocystorhinostomy (DCR). It consists of a long and flexible bicanalicular or monocanalicular tube (e.g., Crawford type) inserted through the lacrimal puncta into the canaliculi, lacrimal sac, and/or nasolacrimal duct; devices to assist the intubation procedure are typically provided preassembled to the tube (e.g., cannula, probes, bougies, introducer, stylet). The tube is typically left in place long-term before removal. This is a single-use device. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 03700773723263 FDA UDI
- FDA Product Code
- OKS FDA UDI
- GMDN Term
- Lacrimal intubation set 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
No
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 intubation set
Lacrijet® 45 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 intubation set.
- Anodyne Surgical — Psi/Eye-Ko, Inc. · U
- V. Mueller — STERIS CORPORATION · Class I
- Novo Surgical — NOVO SURGICAL, INC. · Class I
- Visitec® — Beaver-Visitec International, Inc. · Class I
- Crawford — JEDMED Instrument Company · U
- Lacrimal Intubation Set, Crawford Type — QUEST MEDICAL INC · U
- Crawford — JEDMED Instrument Company · U
- Crawford — JEDMED Instrument Company · 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 b716e84e-ed8a-41e0-acc0-ffd1bc6374ce 33 fields · synced May 30, 2026