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Jamshidi

FDA UDI

Class II (US FDA UDI)

by Carefusion 2200, Inc.

Identity

Trade Name
Jamshidi FDA UDI
Generic Name
Bone marrow biopsy procedure kit FDA UDI
Device Name
Jamshidi Evolve Bone Marrow Biopsy Tray - 11G x 4" EJ Biopsy/Aspiration Needle, Specimen Cradle and 15G TJ Aspiration Needle (Adjustable Length) FDA UDI
Model / Reference
BEJS4511 FDA UDI
Description
Jamshidi Evolve Bone Marrow Biopsy Tray - 11G x 4" EJ Biopsy/Aspiration Needle, Specimen Cradle and 15G TJ Aspiration Needle (Adjustable Length) FDA UDI

Identifiers

Catalog Number
BEJS4511 FDA UDI
Primary DI / UDI-DI
10885403471582 FDA UDI
FDA Product Code
KNW FDA UDI
GMDN Term
Bone marrow biopsy procedure kit 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

Yes

FDA UDI

Combination Product

Yes

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: Bone marrow biopsy procedure kit

Jamshidi by Carefusion 2200, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone marrow biopsy procedure kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI dd3f6447-224d-4e4b-89ca-c06dc4c55cdb 36 fields · synced Sep 18, 2026