AccessGUDID - DEVICE: edelweiss OCCLUSION SET 17-27 L up (09120046322025)

GUDID

Device Identifier (DI) Information

Brand Name: edelweiss OCCLUSION SET 17-27 L up
Version or Model: 13180
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: edelweiss dentistry products gmbh

Primary DI Number: 09120046322025
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 300537672 *Terms of Use

Device Description: SET of total 8 pcs OCCLUSIONS (1x edelweiss OCCLUSION 17 L, 1x edelweiss OCCLUSION 16 L, 1x edelweiss OCCLUSION 15 L, 1x edelweiss OCCLUSION 14 L, 1x edelweiss OCCLUSION 24 L, 1x edelweiss OCCLUSION 25 L, 1x edelweiss OCCLUSION 26 L, 1x edelweiss OCCLUSION 27 L)

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	No
Over the Counter (OTC):	No
Kit:	Yes
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
38645	Dental veneer, professional	A custom-made dental restoration made of ceramic or polymer-based material (resin) intended to be used in aesthetic dentistry to correct the facial surface of a tooth; it is intended to be applied to the teeth by a dental professional for long-term use, typically via an adhesive. This is a single-use device.	Active	false
35870	Dental composite resin	A non-sterile substance intended for professional use as a dental luting agent, liner, base, pulp-capping material, pit/fissure sealant, and/or direct dental restorative material, whereby the majority of the setting reaction is based on the self-, light-, or dual-cured polymerization of a dimethacrylate resin [e.g., polymethylmethacrylate (PMMA), polyurethane, or bisphenol-A-diglycidylether methacrylate (Bis-GMA)]; it includes some additional fillers/components (e.g., glass-based, quartz, or ceramic). It may be preloaded into a syringe, and dedicated disposable devices associated with application may be included. After application, this device cannot be reused.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
EBF	Material, Tooth Shade, Resin

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 6b715023-0343-41ff-b19e-5de65edc4726
Public Version Date: February 05, 2021
Public Version Number: 2
DI Record Publish Date: May 09, 2018