FDA UDI In Commercial Distribution 🇺🇸 United States

SmartPeg Type 38 - Neoss

DI: 09010522002421 · Model: SmartPeg Type 38 - Neoss · Osstell AB
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
SmartPeg Type 38 - Neoss
Primary DI
09010522002421
Version / Model
SmartPeg Type 38 - Neoss
Catalog Number
91071
Company Name
Osstell AB
Labeler DUNS
633171269
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-11-01
Public Version
1
Public Version Date
2023-11-09
Public Version Status
New
Public Device Record Key
023555c1-db7f-48e9-aed5-65816a64c2c8

Device Description

ISQ Measurement Peg

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
EKX Handpiece, Direct Drive, Ac-Powered

GMDN Terms

Code Name
63468 Dental implant stability measurement peg

Identifiers

Type ID
Package 09010522002391
Primary 09010522002421

Premarket Submissions

Submission Number Supplement Number
K181888 000