FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 10885403231803 · Model: BK1000DF · CAREFUSION 2200, INC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
N/A
Primary DI
10885403231803
Version / Model
BK1000DF
Catalog Number
BK1000DF
Company Name
CAREFUSION 2200, INC
Labeler DUNS
832696038
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-21
Public Version
3
Public Version Date
2023-08-01
Public Version Status
Update
Public Device Record Key
53b13e58-bbf2-4ed5-979a-139e6c53b03b

Device Description

Bone Marrow Biopsy Drug Free Tray Without Needle

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LWE Bone marrow collection/transfusion kit

GMDN Terms

Code Name
16833 Bone marrow biopsy procedure kit

Identifiers

Type ID
Package 50885403231801
Primary 10885403231803

Customer Contacts