FDA UDI In Commercial Distribution 🇺🇸 United States

BIOPSYBELL SRL

DI: 08033860024970 · Model: OBSTERN · BIOPSYBELL SRL
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BIOPSYBELL SRL
Primary DI
08033860024970
Version / Model
OBSTERN
Catalog Number
BT1312
Company Name
BIOPSYBELL SRL
Labeler DUNS
438746708
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-14
Public Version
1
Public Version Date
2023-06-22
Public Version Status
New
Public Device Record Key
44d2fcf9-d6bc-4068-8e6a-22271a145f58

Device Description

NEEDLE FOR BONE MARROW EXPLANT

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
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
FCG Biopsy Needle
KNW Instrument, Biopsy

GMDN Terms

Code Name
16833 Bone marrow biopsy procedure kit

Identifiers

Type ID
Primary 08033860024970

Customer Contacts

Phone
+39053527850

Premarket Submissions

Submission Number Supplement Number
K130616 000

Device Sizes

Type Value Unit Text
Needle Gauge 13 Gauge
Length 120 Millimeter