Identity
- Trade Name
- Lacrimal lntubation Set FDA UDI
- Generic Name
- Lacrimal intubation set FDA UDI
- Device Name
- Lacrimal lntubation Set FDA UDI
- Model / Reference
- 6001 FDA UDI
- Description
- Lacrimal lntubation Set FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00845819000359 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Radiation Sterilization FDA UDI
Category: Lacrimal intubation set
A medical device designed for the intubation of the nasolacrimal system, typically used to treat or prevent pathologies such as post-chemotherapy stenosis or dacryocystorhinostomy (DCR).
Similar devices
Also classified as Lacrimal intubation set.
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- 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
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
- OASIS Medical, Inc.
Sources (1)
- FDA UDI 7f4e0a70-90a5-4b66-9263-21c4f7f18997 34 fields · synced Jul 6, 2026