AccessGUDID - DEVICE: Nacera (EDMC45023000030)

GUDID

Device Identifier (DI) Information

Brand Name: Nacera
Version or Model: Hybrid A2 Block M
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 4502300003
Company Name: DOCERAM medical ceramics GmbH

Primary DI Number: EDMC45023000030
Issuing Agency: HIBCC
Commercial Distribution End Date: May 23, 2024
Device Count: 1
Labeler D-U-N-S® Number*: 537713567 *Terms of Use

Device Description: Fully polymerized composite with optimized, high-density filler technology. Radiopaque, 8 shades. Flexural strength: 175 MPa (typical value). Modulus of elasticity: 9900 MPa (typical value).

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:	No
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
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?
16187	Dental appliance fabrication material, ceramic	A dental material made of ceramic materials (e.g., zirconium oxide) intended to be used to manufacture a final dental prosthesis (e.g., a dental implant, removable dentures, crown, bridge) for patient use. It is used to create implantable and removable restorations using manual or computer-aided design/computer-aided manufacturing (CAD/CAM) technology. After application, this material cannot be reused for fabrication.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
EBF	Material, Tooth Shade, Resin
EIH	Powder, Porcelain

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
Storage Environment Temperature: between 5 and 50 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
Device Size Text, specify: 38,8 x 18,9 x 15,5 mm

Device Record Status

Public Device Record Key: 2ae989d9-34eb-4371-9833-f656aa8cb041
Public Version Date: May 24, 2024
Public Version Number: 8
DI Record Publish Date: November 17, 2017