AccessGUDID - DEVICE: TearCare iLid (TM) Device Packaged Pair

GUDID

Device Identifier (DI) Information

Brand Name: TearCare iLid (TM) Device Packaged Pair - 10 pk
Version or Model: FG 05620
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 5-101
Company Name: Sight Sciences, Inc.

Primary DI Number: 10858027006256
Issuing Agency: GS1
Commercial Distribution End Date: August 30, 2019
Device Count: 10
Labeler D-U-N-S® Number*: 962750381 *Terms of Use

Device Description: Eyelid heat therapy system applicator 10 pk

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?
62516	Eyelid heat therapy system applicator	A skin-adherent device intended to be connected to a system control unit to deliver localized heat therapy to the outer eyelid surfaces of an adult patient during treatment of meibomian gland dysfunction (MGD), dry eye syndromes, blepharitis (inflammation of the eyelid), and other related ocular conditions. It consists of an adhesive heat patch/strip that is adhered to the eyelid(s), and typically a cable to allow connection to the control unit. It is intended to be used by a professional in a professional (e.g., clinical) setting. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
IRT	Pad, Heating, Powered

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes 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
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: ef425ea3-71f7-4eb0-8334-4064c021fca5
Public Version Date: August 22, 2023
Public Version Number: 4
DI Record Publish Date: March 16, 2018