FDA UDI In Commercial Distribution 🇺🇸 United States

SPHERO FLEX

DI: 08059224054407 · Model: S/FLEX PRIMA CONNEX ø 4,1 h.5 TiN · RHEIN 83 SRL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
SPHERO FLEX
Primary DI
08059224054407
Version / Model
S/FLEX PRIMA CONNEX ø 4,1 h.5 TiN
Catalog Number
109PRI415R
Company Name
RHEIN 83 SRL
Labeler DUNS
439240722
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-07-08
Public Version
1
Public Version Date
2022-07-18
Public Version Status
New
Public Device Record Key
8f1f1f84-29c2-409b-9978-1c5f0e5af88c

Device Description

Titanium abutment designed as an endosseous dental implant retentive component used to retain a complete or partial denture. The device is screwed into an endosseous implant in the mandible or maxilla.

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 Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
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
NHA Abutment, Implant, Dental, Endosseous

GMDN Terms

Code Name
44879 Dental implant suprastructure, permanent, preformed

Identifiers

Type ID
Primary 08059224054407