Eyelid weight, implantable - An ophthalmic device that is implanted - FCI S A S FCI 20 22

Duns Number:763408366

Device Description: An ophthalmic device that is implanted subcutaneously within the upper eyelid to "lidload" An ophthalmic device that is implanted subcutaneously within the upper eyelid to "lidload" the eyelid to restore upper eyelid muscle (musculus orbicularis oculi) function. This device is used for the treatment of lagophthalmos, a condition that frequently results from facial paralysis caused by Bell's palsy, trauma, a stroke, or as an indirect consequence of the surgical removal of certain types of tumour in close proximity to the facial nerve. This device uses gravity to gently close the upper eyelid when blinking or when the eyelid muscle is relaxed, and is made of a heavy material [e.g., gold (Au), platinum (Pt)].

Want to know more about this Product? Request more information now!


More Product Details

Catalog Number

S3.1000u

Brand Name

Eyelid weight, implantable

Version/Model Number

PTOSIS SLING SET LLOUQUET & GUERIN, M. D.

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

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)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code Details

Product Code

HJZ

Product Code Name

Crutch, Ptosis

Device Record Status

Public Device Record Key

dc5c735c-9186-4cd2-ac85-5b8a8353b61d

Public Version Date

March 05, 2020

Public Version Number

1

DI Record Publish Date

February 26, 2020

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"FCI S A S FCI 20 22" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 82
2 A medical device with a moderate to high risk that requires special controls. 291
U Unclassified 60