Identity
- Trade Name
- Lacrimal Instruments FDA UDI
- Generic Name
- Lacrimal dilator, reusable FDA UDI
- Device Name
- SOFT PLUG® Punctal Plug Gauge Set, 0.5mm/0.6mm and 0.7mm/0.8mm FDA UDI
- Model / Reference
- 6630 FDA UDI
- Description
- SOFT PLUG® Punctal Plug Gauge Set, 0.5mm/0.6mm and 0.7mm/0.8mm FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00845819005156 FDA UDI
- FDA Product Code
- HNW FDA UDI
- GMDN Term
- Lacrimal dilator, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.4350 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
Category: Lacrimal dilator, reusable
Lacrimal Instruments by OASIS Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Lacrimal dilator, reusable.
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- Ambler Surgical — Ambler Surgical, LLC · Class I
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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
- OASIS Medical, Inc.
Sources (1)
- FDA UDI 2106678b-c3ed-4671-ac6f-982885867ce1 34 fields · synced Jun 9, 2026