AccessGUDID - DEVICE: REFRESH RELIEVA FOR CONTACTS (00300236632083)

GUDID

Device Identifier (DI) Information

Brand Name: REFRESH RELIEVA FOR CONTACTS
Version or Model: 96632
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: Allergan, Inc.

Primary DI Number: 00300236632083
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 144796497 *Terms of Use

Device Description: REFRESH RELIEVA FOR CONTACTS Lubricant Eye Drops

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:	No
Prescription Use (Rx):	No
Over the Counter (OTC):	Yes
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?
44237	Eye lubricant	A substance intended to provide supplemental lubrication/hydration to the natural eye to treat dry, tired, irritated, and/or strained eyes resulting from dry eye syndrome, ageing/hormone changes (menopause), or environmental factors (e.g., medications, pollution, computer use, air conditioning, allergy); some types may in addition be intended to wet contact lenses during wear. It may be a topical solution, spray, suspension, or gel applied to the eyes or eyelids, and may have special formulations (e.g., intensive, night use). It is intended for use in the home or healthcare facility (single dose or multidose). After application, this device cannot be reused.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LPN	Accessories, Soft Lens Products

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K190674	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 59 and 86 Degrees Fahrenheit

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 6203d410-1f05-4d30-a0bb-a24be6d7613e
Public Version Date: November 06, 2020
Public Version Number: 2
DI Record Publish Date: August 27, 2019

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
No Package DIs found

Secondary DI

[?]

Issuing Agency [?]	Secondary DI Number
No Secondary DIs found

Unit of Use DI

[?]

Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]

Device Subject to Direct Marking (DM), but Excepted: No
DM DI Different from Primary DI: No
DM DI Number: None
CLOSE

Production Identifier(s) in UDI

[?]

Lot or Batch Number: Yes
Serial Number: Yes
Expiration Date: Yes
Manufacturing Date: No
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: 18006781605
Email: ProductSupport@allergan.com

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