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MPD Lancet Ultra Thin (Box of 100)

FDA UDI

Class II (US FDA UDI)

by Medical Plastic Devices M.P.D. Inc

Identity

Trade Name
MPD Lancet Ultra Thin (Box of 100) FDA UDI
Generic Name
Blood lancet, single-use FDA UDI
Device Name
MPD Lancets Ultra Thin. 3 Bevel point, sterile tip. Single Use. Box of 100 Color Purple Sterilized by Radiation FDA UDI
Model / Reference
1 FDA UDI
Description
MPD Lancets Ultra Thin. 3 Bevel point, sterile tip. Single Use. Box of 100 Color Purple Sterilized by Radiation FDA UDI

Identifiers

Catalog Number
P0361 FDA UDI
Primary DI / UDI-DI
00628465003611 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 Ultra Thin (Box of 100) by Medical Plastic Devices M.P.D. Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood lancet, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 395252cf-c58d-4763-a59f-1ff21780fe24 35 fields · synced May 30, 2026