FDA UDI In Commercial Distribution 🇺🇸 United States

Hi-Rem+ # 3

DI: 08059388441686 · Model: Hi-Rem+ # 3 · OVERFIBERS SRL
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
Hi-Rem+ # 3
Primary DI
08059388441686
Version / Model
Hi-Rem+ # 3
Catalog Number
RHP603
Company Name
OVERFIBERS SRL
Labeler DUNS
431704826
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2025-03-12
Public Version
1
Public Version Date
2025-03-20
Public Version Status
New
Public Device Record Key
52dc41f3-49d9-4662-9ec9-00cd1deb61d3

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
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
ELR Post, Root Canal

GMDN Terms

Code Name
38609 Root canal post, preformed

Identifiers

Type ID
Unit of Use 08059388443291
Primary 08059388441686

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep away from heat, moisture and direct sunlight