Identity
- Trade Name
- Vein Pick FDA UDI
- Generic Name
- Vein pick FDA UDI
- Device Name
- Vein Pick FDA UDI
- Model / Reference
- VP52Y FDA UDI
- Description
- Vein Pick FDA UDI
Identifiers
- Catalog Number
- VP52Y FDA UDI
- Primary DI / UDI-DI
- 40836559009250 FDA UDI
- 510(k) Number
- K024053 FDA UDI
- FDA Product Code
- DTB FDA UDI
- GMDN Term
- Vein pick FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Regulation Number
- 870.3680 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Length — 45 Millimeter FDA UDI
Category: Vein pick
Vein Pick by Oscor Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Vein pick.
- Wexler Surgical, Inc. — Wexler Surgical, Inc. · Class I
- VL — BIOTRONIK SE & Co. KG · Class III
- Vein Pick — Oscor Inc. · Class III
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 III | Pending data |
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Manufacturer
- Manufacturer
- Oscor Inc.
Sources (1)
- FDA UDI 5b2097e5-997b-4036-b1d7-e99c563862a1 38 fields · synced Jun 6, 2026