FDA UDI In Commercial Distribution 🇺🇸 United States

LUKE BX Single Use Biopsy Forceps

DI: 00810024670284 · Model: BFC-MD-000650 · CENTERPOINT SYSTEMS LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
LUKE BX Single Use Biopsy Forceps
Primary DI
00810024670284
Version / Model
BFC-MD-000650
Company Name
CENTERPOINT SYSTEMS LLC
Labeler DUNS
117126091
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-07-22
Public Version
1
Public Version Date
2024-07-30
Public Version Status
New
Public Device Record Key
decb77f6-44b2-4697-9929-14e252b7891e

Device Description

Single-use Biopsy Forceps

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FCL Forceps, Biopsy, Non-Electric

GMDN Terms

Code Name
38711 Flexible endoscopic biopsy forceps, single-use

Identifiers

Type ID
Primary 00810024670284