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Medichoice

FDA UDI

Class II (US FDA UDI)

by Owens & Minor Distribution, Inc.

Identity

Trade Name
Medichoice FDA UDI
Generic Name
Bone marrow collection/transfusion set FDA UDI
Device Name
X Rx Tray Aspiration Bone Marrow Biopsy With Needle Single-Patient Use Latex-Free Sterile MediChoice FDA UDI
Model / Reference
BMA652 FDA UDI
Description
X Rx Tray Aspiration Bone Marrow Biopsy With Needle Single-Patient Use Latex-Free Sterile MediChoice FDA UDI

Identifiers

Primary DI / UDI-DI
10885632107795 FDA UDI
510(k) Number
K061570 FDA UDI
FDA Product Code
KNW FDA UDI
GMDN Term
Bone marrow collection/transfusion set 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

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

Category: Bone marrow collection/transfusion set

Medichoice by Owens & Minor Distribution, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone marrow collection/transfusion set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6633a074-115b-4e50-a8d5-cd4e3c36c1cc 35 fields · synced Jun 8, 2026