Identity
- Trade Name
- MPD Lancet FDA UDI
- Generic Name
- Blood lancet, single-use FDA UDI
- Device Name
- MPD Lancets Thin. 3 Bevel point, sterile tip. Single Use. 23 Guage Box of 100 Color Blue Sterilized by Radiation FDA UDI
- Model / Reference
- Thin 23Ga FDA UDI
- Description
- MPD Lancets Thin. 3 Bevel point, sterile tip. Single Use. 23 Guage Box of 100 Color Blue Sterilized by Radiation FDA UDI
Identifiers
- Catalog Number
- P0351 FDA UDI
- Primary DI / UDI-DI
- 00628465003512 FDA UDI
- FDA Product Code
- FMK FDA UDI
- GMDN Term
- Blood lancet, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4850 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
No
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Blood lancet, single-use
MPD Lancet by Medical Plastic Devices M.P.D. Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Blood lancet, single-use.
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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 II | Pending data |
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Manufacturer
- Manufacturer
- Medical Plastic Devices M.P.D. Inc
Sources (1)
- FDA UDI 2bfc1568-5b0d-43dc-b824-b68aff024e31 35 fields · synced May 30, 2026