Identity
- Trade Name
- No-Scalpel Vasectomy FDA UDI
- Generic Name
- Urological surgical procedure kit, non-medicated, reusable FDA UDI
- Device Name
- No-Scalpel Vasectomy 3.5mm kit FDA UDI
- Model / Reference
- 3.5mm Kit FDA UDI
- Description
- No-Scalpel Vasectomy 3.5mm kit FDA UDI
Identifiers
- Catalog Number
- LV-03K-856 FDA UDI
- Primary DI / UDI-DI
- 15055515600278 FDA UDI
- FDA Product Code
- KOA FDA UDI
- GMDN Term
- Urological surgical procedure kit, non-medicated, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 876.4730 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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Lumen/Inner Diameter — 3.5 Millimeter FDA UDI
Category: Urological surgical procedure kit, non-medicated, reusable
No-Scalpel Vasectomy by Femcare , Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Urological surgical procedure kit, non-medicated, reusable.
- KNUTSON URETHROGRAPHY SET — SONTEC INSTRUMENTS, INC. · Class I
- No-Scalpel Vasectomy — Femcare , Ltd. · Class I
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
- Femcare , Ltd.
Sources (1)
- FDA UDI b7b08519-b99b-4c2e-b822-8a017e2c1b1b 35 fields · synced May 30, 2026