Identity
- Trade Name
- Lacrimal lntubation Set FDA UDI
- Generic Name
- Lacrimal intubation set FDA UDI
- Device Name
- Lacrimal Intubation Set with Retrieval Device FDA UDI
- Model / Reference
- 6004 FDA UDI
- Description
- Lacrimal Intubation Set with Retrieval Device FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00845819000311 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
Lacrimal lntubation Set by OASIS Medical, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Lacrimal intubation set.
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- 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 47f0223b-7d35-4bba-a7b0-33fc0d7be5c5 34 fields · synced Jun 9, 2026