FDA UDI In Commercial Distribution 🇺🇸 United States

Neoss Implant System

DI: 05060440332128 · Model: 41182 · Neoss AB
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Neoss Implant System
Primary DI
05060440332128
Version / Model
41182
Catalog Number
41182
Company Name
Neoss AB
Labeler DUNS
509583543
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-01
Public Version
5
Public Version Date
2021-05-10
Public Version Status
Update
Public Device Record Key
48e91eba-5bd9-4c92-b0ec-7d5b4d7db577

Device Description

Countersink, Tapered Ø5.5 mm

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
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
DZI Drill, Bone, Powered

GMDN Terms

Code Name
16462 Surgical countersink, reusable

Identifiers

Type ID
Primary 05060440332128

Customer Contacts

Phone
999-999-9999