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BD MiniDraw™ Finger Sleeve, Large

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD MiniDraw™ Finger Sleeve, Large FDA UDI
Generic Name
Capillary blood collection funnel FDA UDI
Device Name
BD MiniDraw™ Finger Sleeve, Large FDA UDI
Model / Reference
366615 FDA UDI
Description
BD MiniDraw™ Finger Sleeve, Large FDA UDI

Identifiers

Catalog Number
366615 FDA UDI
Primary DI / UDI-DI
50382903666152 FDA UDI
510(k) Number
K230391 FDA UDI
K230493 FDA UDI
FDA Product Code
GIM FDA UDI
JKA FDA UDI
GMDN Term
Capillary blood collection funnel FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1675 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Category: Capillary blood collection funnel

BD MiniDraw™ Finger Sleeve, Large by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Capillary blood collection funnel.

Cleared under the same submission

K230391 also covers:

K230493 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 d6b132b7-cf0b-40eb-91b0-550449ba2b54 36 fields · synced May 30, 2026