DEVICE: FIBRAPOST PLUS N°1-4 (24 glass fibre posts + 4 reamers + 1 screwdiver) (07640159162889)
Device Identifier (DI) Information
FIBRAPOST PLUS N°1-4 (24 glass fibre posts + 4 reamers + 1 screwdiver)
22595
In Commercial Distribution
Produits dentaires S.A.
22595
In Commercial Distribution
Produits dentaires S.A.
Core build up - 6 posts + 1 reamer RA of each #1-4 -
N°1
Total Length 19mm
Length of tapered part 11mm
Diameter of the lower tip 0.85mm
Diameter of the cylindrical part 1.30mm
N°2
Total Length 19mm
Length of tapered part 11mm
Diameter of the lower tip 1.06mm
Diameter of the cylindrical part 1.50mm
N°3
Total Length 19mm
Length of tapered part 11mm
Diameter of the lower tip 1.26mm
Diameter of the cylindrical part 1.70mm
N°4
Total Length 19mm
Length of tapered part 11mm
Diameter of the lower tip 1.47mm
Diameter of the cylindrical part 1.90mm
Device Characteristics
Labeling does not contain MRI Safety Information | |
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No | |
No | |
Yes | |
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No |
GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
---|---|---|---|---|
38609 | Root canal post, preformed |
A prefabricated endodontic rod designed for insertion into the root canal of a patient to support and retain a crown prosthesis. It is typically a solid, cylindrical, metal (e.g., stainless steel, gold alloy) piece with a proximal end appropriate to support the crown on top; it is, however, available in a variety of shapes, dimensions, and materials (e.g., ceramics, fibre-reinforced polymers). In addition, it is available in a variety of types (e.g., non-threaded, pre-threaded, or self-tapping; straight or tapered). This is a single-use device.
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Active | false |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
ELR | Post, Root Canal |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
---|---|
Premarket Submission Number Not Available/Not Released |
Sterilization
Storage and Handling
[?]Storage and Handling |
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No storage/handling found |
Clinically Relevant Size
[?]Size Type Text |
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No Device Sizes |
Device Record Status
68bfa57a-2cb1-4fe7-a8ab-eb1af24a7843
June 30, 2022
1
June 22, 2022
June 30, 2022
1
June 22, 2022
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
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No Package DIs found |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
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No Secondary DIs found |
Unit of Use DI
[?]
Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
+41219212631
info@pd-dental.com
info@pd-dental.com