Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Lacrimal dilator, reusable FDA UDI
- Device Name
- V. Mueller RUEDEMAN LACRIMAL DILATOR, 12MM TAPER, NEEDLE TYPE TIP, ROUND, SMOOTH HANDLE SHORT FDA UDI
- Model / Reference
- OP0918-501 FDA UDI
- Description
- V. Mueller RUEDEMAN LACRIMAL DILATOR, 12MM TAPER, NEEDLE TYPE TIP, ROUND, SMOOTH HANDLE SHORT FDA UDI
Identifiers
- Catalog Number
- OP0918501 FDA UDI
- Primary DI / UDI-DI
- 10885403160141 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
V. Mueller by Steris Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Steris Corporation
Sources (1)
- FDA UDI 8450b787-e827-4752-a3e8-dd71ad6dc0f6 35 fields · synced Jun 8, 2026