FDA UDI In Commercial Distribution 🇺🇸 United States

BIOPSY NEEDLE

DI: 00812444022926 · Model: RP1000-1825 · RIVERPOINT MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
BIOPSY NEEDLE
Primary DI
00812444022926
Version / Model
RP1000-1825
Company Name
RIVERPOINT MEDICAL, LLC
Labeler DUNS
964053560
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
a8146b17-26ea-4927-b200-b87eb02acb6c

Device Description

BIOPSY NEEDLE

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
No
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
KNW Instrument, Biopsy

GMDN Terms

Code Name
57796 Prostate biopsy needle

Identifiers

Type ID
Primary 00812444022926
Package 10812444022923

Premarket Submissions

Submission Number Supplement Number
K092059 000