FDA UDI In Commercial Distribution 🇺🇸 United States

Tuff PRO Implant

DI: 07290116151335 · Model: NM1F3311 · NORIS MEDICAL LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Tuff PRO Implant
Primary DI
07290116151335
Version / Model
NM1F3311
Catalog Number
NM1F3311
Company Name
NORIS MEDICAL LTD
Labeler DUNS
649340106
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-03-24
Public Version
1
Public Version Date
2025-04-01
Public Version Status
New
Public Device Record Key
6d0be86c-5bd7-4e97-8741-b246bcdc25e9

Device Description

Tuff PRO, D3.3, L11.5, Int. Hex Ti. Implant

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 Conditional
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
DZE Implant, Endosseous, Root-Form

GMDN Terms

Code Name
55849 Screw endosteal dental implant, two-piece

Identifiers

Type ID
Primary 07290116151335

Customer Contacts