AccessGUDID - DEVICE: Hydroxyapatite Orbital Implant (05060171621904)

GUDID

Device Identifier (DI) Information

Brand Name: Hydroxyapatite Orbital Implant
Version or Model: SP22
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number:
Company Name: CERAMISYS LTD

Primary DI Number: 05060171621904
Issuing Agency: GS1
Commercial Distribution End Date: October 20, 2021
Device Count: 1
Labeler D-U-N-S® Number*: 423459374 *Terms of Use

Device Description: Porous Hydroxyapatite Orbital Implant, Sphere, 22mm

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?
46902	Orbital sphere implant	An implantable ocular device designed to permanently fill the orbital cavity following enucleation, evisceration, or after the removal of another ocular implant (used as a secondary implant), to replace the volume and possibly, given the surgical method, to impart motion to the eventual ocular prosthesis (the artificial eyeball). It is typically aspherical and may have porous surfaces to facilitate colonization by fibrovascular tissue to offer the advantages of reduced risk of infection or implant extrusion. It is available in various sizes and is typically made of polymethylmethacrylate (PMMA), poly 2-hydroxyethylmethacrylate (PHEMA), or silicone.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
HPZ	Implant, Eye Sphere

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K110554	000

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
Storage Environment Temperature: between 15 and 25 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 61c31702-69a4-4eb8-8bfb-b090389e0f6c
Public Version Date: October 21, 2021
Public Version Number: 4
DI Record Publish Date: July 31, 2015