FDA UDI In Commercial Distribution 🇺🇸 United States

E-FIBER

DI: 07898078659274 · Model: E-FIBER 10 cm 1.2 mm · Angelus Industria de Produtos Odontologicos S A
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
E-FIBER
Primary DI
07898078659274
Version / Model
E-FIBER 10 cm 1.2 mm
Catalog Number
4432
Company Name
Angelus Industria de Produtos Odontologicos S A
Labeler DUNS
906943303
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-02-17
Public Version
1
Public Version Date
2025-02-25
Public Version Status
New
Public Device Record Key
707021f9-7f63-4340-a050-15d74198eaae

Device Description

Fiberglass material used for the reinforcement of dental prostheses and the splinting of teeth.

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EBI Resin, Denture, Relining, Repairing, Rebasing

GMDN Terms

Code Name
44786 Dental reinforcing fibre

Identifiers

Type ID
Primary 07898078659274

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K082180 000