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BD Microtainer® Contact-Activated Lancet

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Microtainer® Contact-Activated Lancet FDA UDI
Generic Name
Manual blood lancing device, single-use FDA UDI
Device Name
LANCET CONT-ACT PURPLE 30GX1.5MM FDA UDI
Model / Reference
366592 FDA UDI
Description
LANCET CONT-ACT PURPLE 30GX1.5MM FDA UDI

Identifiers

Catalog Number
366592 FDA UDI
Primary DI / UDI-DI
30382903665922 FDA UDI
510(k) Number
K223243 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Needle Gauge — 30.00 Gauge FDA UDI

BD Microtainer® Contact-Activated Lancet by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K223243 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Becton Dickinson And Company

Sources (1)

  • FDA UDI af2b1e4d-8ab6-489a-a323-b2fcc6913c27 38 fields · synced May 31, 2026