Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Lacrimal dilator, reusable FDA UDI
- Device Name
- NETTLESHIP-WILDER LACRIMAL DILATOR LONG, DELICATE TAPER OVERALL LENGTH 4" (10.2CM) FDA UDI
- Model / Reference
- OP6972 FDA UDI
- Description
- NETTLESHIP-WILDER LACRIMAL DILATOR LONG, DELICATE TAPER OVERALL LENGTH 4" (10.2CM) FDA UDI
Identifiers
- Catalog Number
- OP6972 FDA UDI
- Primary DI / UDI-DI
- 10885403099922 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
- Not 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
V. Mueller by Carefusion 2200, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Carefusion 2200, Inc.
Sources (1)
- FDA UDI 582066ca-e7ea-41cb-890f-e94c862218f1 36 fields · synced Sep 18, 2026