Identity
- Trade Name
- MSI Precision Specialty Instruments FDA UDI
- Generic Name
- Lacrimal dilator, reusable FDA UDI
- Device Name
- Castroviejo Lacrimal Dilator, Double Ended, Needle Point 0.25mm One End, Medium Taper 0.75mm Tip x 13mm Long Other End, Round Knurled Handle, Polished Finish, Stainless Steel, Overall Length 5-1/2" (14mm) FDA UDI
- Model / Reference
- 5-5451-E FDA UDI
- Description
- Castroviejo Lacrimal Dilator, Double Ended, Needle Point 0.25mm One End, Medium Taper 0.75mm Tip x 13mm Long Other End, Round Knurled Handle, Polished Finish, Stainless Steel, Overall Length 5-1/2" (14mm) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00194613083168 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
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Lacrimal dilator, reusable
MSI Precision Specialty Instruments by Med Saver, 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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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
- Med Saver, Inc.
Sources (1)
- FDA UDI 2b9060a2-21c2-4a37-a680-b3fcc2414fae 34 fields · synced May 30, 2026