FDA UDI In Commercial Distribution 🇺🇸 United States

Yomi One Implant System

DI: 05060967630233 · Model: 54002 · Neoss AB
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Yomi One Implant System
Primary DI
05060967630233
Version / Model
54002
Catalog Number
54002
Company Name
Neoss AB
Labeler DUNS
509583543
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-02-15
Public Version
1
Public Version Date
2024-02-23
Public Version Status
New
Public Device Record Key
f2e50e55-2936-4e5d-9017-92590244451c

Device Description

Surgical and Prosthetic Tray

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
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
12143 Instrument tray, reusable

Identifiers

Type ID
Direct Marking 05060440335853
Primary 05060967630233

Customer Contacts

Phone
999-999-9999