Identity
- Trade Name
- MiniCollect FDA UDI
- Generic Name
- Manual blood lancing device, single-use FDA UDI
- Device Name
- MiniCollect® Lancelino Safety Lancet 25G penetration depth 1,50 mm lavender, sterile, for capillary blood collection with needle FDA UDI
- Model / Reference
- 450521 FDA UDI
- Description
- MiniCollect® Lancelino Safety Lancet 25G penetration depth 1,50 mm lavender, sterile, for capillary blood collection with needle FDA UDI
Identifiers
- Catalog Number
- 450521 FDA UDI
- Primary DI / UDI-DI
- 29120049202212 FDA UDI
- FDA Product Code
- FMK FDA UDI
- GMDN Term
- Manual blood lancing device, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4850 FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MiniCollect by Greiner Bio-One GmbH — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Greiner Bio-One GmbH
Sources (1)
- FDA UDI 3650d79d-8dd5-4438-a4e5-84b993118a12 36 fields · synced May 30, 2026