Jamshidi

FDA UDI

Class I (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 (TJ) SAFE-T PLUS BM TRAY 11GMAC FDA UDI
Model / Reference: BCTM3411SP FDA UDI
Description: JAMSHIDI (TJ) SAFE-T PLUS BM TRAY 11GMAC FDA UDI

Identifiers

Catalog Number: BCTM3411SP FDA UDI
Primary DI / UDI-DI: 10885403107702 FDA UDI
FDA Product Code: KNM FDA UDI
GMDN Term: Bone marrow biopsy procedure kit FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 890.5765 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Needle Gauge — 11 Gauge FDA UDI
Length — 4 Inch FDA UDI

Category: Bone marrow biopsy procedure kit

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Carefusion 2200, Inc.

Sources (1)

FDA UDI 7b50615d-47d9-444f-b104-6b4fcd992fa7 36 fields · synced Sep 18, 2026