FDA UDI Not in Commercial Distribution 🇺🇸 United States

Mark

DI: 08052440107490 · Model: PNX2012 · M.D.L. S.R.L.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Mark
Primary DI
08052440107490
Version / Model
PNX2012
Catalog Number
PNX2012
Company Name
M.D.L. S.R.L.
Labeler DUNS
447228586
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-06-05
Public Version
6
Public Version Date
2021-05-27
Public Version Status
Update
Public Device Record Key
077940a7-fb6f-469e-ad21-37557917524f
Distribution End Date
2021-04-26

Device Description

NOT REPOSITIONABLE NEEDLE 20G X 120mm FOR MAMMARY NODULES LOCALIZATION WITH DOUBLE HOOK

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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GDF Guide, Needle, Surgical

GMDN Terms

Code Name
46350 Bone marrow biopsy needle, single-use

Identifiers

Type ID
Package 08058341214022
Primary 08052440107490

Device Sizes

Type Value Unit Text
Needle Gauge 20 Gauge
Length 120 Millimeter