AccessGUDID - DEVICE: EAGLE VISION COLLAGEN INSERTS (00844505004411)

GUDID

Device Identifier (DI) Information

Brand Name: EAGLE VISION COLLAGEN INSERTS
Version or Model: 0026
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number:
Company Name: EAGLE VISION, INC.

Primary DI Number: 00844505004411
Issuing Agency: GS1
Commercial Distribution End Date: March 31, 2017
Device Count: 1
Labeler D-U-N-S® Number*: 174318360 *Terms of Use

Device Description: EAGLE VISION COLLAGEN INSERTS 0.3MM DIAMETER X 2.0MM LENGTH

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?
36237	Lacrimal punctum plug	A sterile device inserted into a punctal opening to prevent tear outflow in dry eye patients. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LZU	Plug, Punctum

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
No Device Sizes

Device Record Status

Public Device Record Key: 12808f2a-499f-4104-8864-2e765d866cf2
Public Version Date: March 29, 2018
Public Version Number: 2
DI Record Publish Date: September 26, 2016