AccessGUDID - DEVICE: DD Prefab Starter Kit (EDDICAM110151)

GUDID

Device Identifier (DI) Information

Brand Name: DD Prefab Starter Kit
Version or Model: SilaMill N4
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: CAM 1101.5
Company Name: Dental Direkt GmbH

Primary DI Number: EDDICAM110151
Issuing Agency: HIBCC
Commercial Distribution End Date: February 20, 2024
Device Count: 3
Labeler D-U-N-S® Number*: 313214171 *Terms of Use

Device Description: The DD Prefab Starter Kit SilaMill N4 contains one SilaMill N4 holder, one bar, four black M4 screws, three silver M4 screws, one screwdriver SW 3mm, three calibration bodies and three prefabs.

Device Characteristics

What MRI safety information does the labeling contain?	MR Conditional
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):	Yes
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?
44879	Dental implant suprastructure, permanent, preformed	A prefabricated device intended to provide a permanent intermediate fixture level between a dental implant and the final prosthesis/restoration (e.g., bridge, single tooth, overdenture). It includes one or more structural component(s) [e.g., abutment, ball, bar, bar overlay, coping, ring], and may be made of various materials [e.g., titanium (Ti), plastic, gold alloy]. It includes devices glued to prostheses and/or devices that can be replaced during cleaning cycles. An abutment screw(s) may be included, however the suprastructure does not represent the screw(s) in isolation. It may also be referred to as an abutment assembly or mesostructure.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
NHA	Abutment, Implant, Dental, Endosseous

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: Yes

Sterilization Method [?]
Moist Heat or Steam Sterilization

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: a2456fbd-3ef6-4045-a320-7f940865bf4c
Public Version Date: February 27, 2024
Public Version Number: 1
DI Record Publish Date: February 19, 2024