FDA UDI In Commercial Distribution 🇺🇸 United States

Neoss Implant System

DI: 05060440332500 · Model: 41203 · Neoss Ltd
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Neoss Implant System
Primary DI
05060440332500
Version / Model
41203
Catalog Number
41203
Company Name
Neoss Ltd
Labeler DUNS
216693627
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-05
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
1d5de24c-067d-4232-9aab-c709718dd1d4

Device Description

X-ray Planner Ø6.0 Implants

Device Characteristics

Single Use
No
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
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
NDP Accessories, Implant, Dental, Endosseous

GMDN Terms

Code Name
44883 Dental implant/prosthesis surgical procedure kit

Identifiers

Type ID
Primary 05060440332500

Customer Contacts

Phone
999-999-9999