FDA UDI In Commercial Distribution 🇺🇸 United States

PrimoCut

DI: 14048223016418 · Model: 415S120100 · Pajunk GmbH Medizintechnologie
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
PrimoCut
Primary DI
14048223016418
Version / Model
415S120100
Catalog Number
415S120100
Company Name
Pajunk GmbH Medizintechnologie
Labeler DUNS
317654283
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2016-12-15
Public Version
4
Public Version Date
2021-03-16
Public Version Status
Update
Public Device Record Key
0452b477-62d9-4d51-aaec-e05a33edc828
Distribution End Date
2025-03-15

Device Description

PrimoCut 18G (1,2) x 100mm sterile

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
MR Unsafe
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
MJG DEVICE, PERCUTANEOUS, BIOPSY

GMDN Terms

Code Name
58990 Side-notch biopsy gun handpiece/needle

Identifiers

Type ID
Primary 14048223016418
Unit of Use 04048223016411

Customer Contacts