FDA UDI In Commercial Distribution 🇺🇸 United States

Neoss Implant System

DI: 05060440331671 · Model: 41112 · Neoss AB
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Neoss Implant System
Primary DI
05060440331671
Version / Model
41112
Catalog Number
41112
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
a29c3006-6524-494a-bdf1-3dc1ddd533c6

Device Description

Countersink, Straight Ø4.5

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 05060440331671

Customer Contacts

Phone
999-999-9999