Senture, surgical guide

Primary DI
06972677871655
Brand
Senture, surgical guide
Company
Modern Dental Laboratory (DG) Co., Ltd.
Model
164
Published
2020-07-21
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
true

Product Codes#

Code, Name table
CodeName
NDPAccessories, Implant, Dental, Endosseous

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
NDPAccessories, Implant, Dental, EndosseousDental1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
06972677871648PrimaryGS10
06972677871655Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
06972677871648069726778716486972677871648
06972677871655069726778716556972677871655

GMDN Terms#

Term, Definition table
TermDefinition
Custom-made orthopaedic surgical guide, non-sterileA non-sterile, custom-made surgical instrument intended to be used in an orthopaedic and/or craniomaxillofacial procedure (e.g., osteotomy, arthroplasty, tumour resection, distraction osteogenesis, cranial vault reconstruction) to assist in the intraoperative orientation of implant components, outlining the desired cut-line, and/or guiding of surgical instruments (e.g., surgical drill, oscillating cutting saw). It is made of synthetic polymer materials and is typically manufactured by 3-D printing and CAD/CAM techniques to match the patient-specific contours of the target anatomical site. This is a single-use device intended to be sterilized prior to use.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
551746187
Device count
2
DM exempt
true
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
06972677870214Trioclear System S,H2023-09-04
06972677870221Trioclear SystemS2023-09-04
06972677870238Trioclear SystemH2023-09-04
06972677870207Orthodontic Appliance0202023-08-08
06972677870191Respire Pink AT Series0192022-09-19
06972677871877Respire Pink AT Series,Retainer1862022-09-19
06972677871891Respire Pink AT Series,Splint1882022-09-19
06972677870153Blue Series0152022-08-26
06972677870160Pink Series0162022-08-26
06972677870177Blue EF Series0172022-08-26
06972677870184Pink EF Series0182022-08-26
06972677871730Pink Series,Retainer1722022-08-26
06972677871754Blue EF Series,Retainer1742022-08-26
06972677871778Pink EF Series,Retainer1762022-08-26
06972677871792Blue Series,Splint1782022-08-26
06972677871815Pink Series,Splint1802022-08-26
06972677871839Blue EF Series,Splint1822022-08-26
06972677871853Pink EF Series,Splint1842022-08-26
06972677871662Moses appliance,Dentures, partial1662022-08-18
06972677871693EMA appliance,Dentures, partial1682022-08-18

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