AccessGUDID - DEVICE: PMMA (00858174006003)

GUDID

Device Identifier (DI) Information

Brand Name: PMMA
Version or Model: 003
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: LAGADO CORPORATION, THE

Primary DI Number: 00858174006003
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 109884150 *Terms of Use

Device Description: PMMA (polymethyl methacrylate) hard contact lens for daily wear

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?
47839	Hard corrective contact lens	A rigid ophthalmic lens intended to be worn directly against the cornea of the eye to correct refractive vision conditions (e.g., myopia, hyperopia, astigmatism, presbyopia). The device is made of polymethylmethacrylate (PMMA), also known as Plexiglas or Lucite, and does not permit diffusion of oxygen (O2) to the ocular surface. These lenses are virtually obsolete and rarely used. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
HPX	Lens, Contact (Polymethylmethacrylate)

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K895411	000

Device Exempt from Premarket Submission: No 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: 73399476-58cb-47ab-a9a2-2ac48efda11e
Public Version Date: July 06, 2018
Public Version Number: 3
DI Record Publish Date: July 29, 2016

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: No
Expiration Date: No
Manufacturing Date: No
Donation Identification Number: No CLOSE

Customer Contact

[?]

No Customer Contact currently defined

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