AccessGUDID - DEVICE: GUIDOR easy-graft CLASSIC (07640164364544)

GUDID

Device Identifier (DI) Information

Brand Name: GUIDOR easy-graft CLASSIC
Version or Model: C11-018
Commercial Distribution Status: In Commercial Distribution
Catalog Number: C11-018
Company Name: Degradable Solutions AG

Primary DI Number: 07640164364544
Issuing Agency: GS1
Commercial Distribution End Date: April 18, 2027
Device Count: 1
Labeler D-U-N-S® Number*: 482821667 *Terms of Use
Previous DI: 07640164360089

Device Description: in situ hardening synthetic bone graft system, 0.15 Milliliter

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):	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?
47971	Dental bone matrix implant, synthetic	A sterile bioabsorbable device made of synthetic material implanted into the body to provide osteoconductive bone-tissue scaffolds to replace maxillofacial and/or mandibular bone lost through trauma or dental surgery. It is typically made of ceramics (e.g., tricalcium phosphate or hydroxyapatite), sometimes bioactive glasses or bioabsorbable polymers, and used to fill bone cavities and defects to promote the ingrowth of endogenous bone for skeletal reconstruction and/or augmentation. It is typically provided as sterile cancellous blocks, chips, or granules of varying sizes, or mouldable materials.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
LYC	Bone Grafting Material, Synthetic

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: Yes
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
Total Volume: 0.15 Milliliter

Device Record Status

Public Device Record Key: ae293aa4-cc3e-41a6-a7aa-de92490b57bb
Public Version Date: May 28, 2025
Public Version Number: 2
DI Record Publish Date: May 02, 2022