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Monoject

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Monoject FDA UDI
Generic Name
Bone marrow biopsy needle, single-use FDA UDI
Device Name
Snarecoil Bone Marrow Biopsy Needle FDA UDI
Model / Reference
SC6011X FDA UDI
Description
Snarecoil Bone Marrow Biopsy Needle FDA UDI

Identifiers

Catalog Number
SC6011X FDA UDI
Primary DI / UDI-DI
10884521021112 FDA UDI
510(k) Number
K983187 FDA UDI
FDA Product Code
KNW FDA UDI
GMDN Term
Bone marrow biopsy needle, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1075 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

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 6 Inch FDA UDI

Category: Bone marrow biopsy needle, single-use

Monoject by Cardinalhealth — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone marrow biopsy needle, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI aa57c603-801a-49e4-88ad-0c63ebce0816 38 fields · synced May 30, 2026