VitreQ - 25G Forceps, Eckardt Endgripping - Vitreq B.V.

Duns Number:491393613

Device Description: 25G Forceps, Eckardt Endgripping

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More Product Details

Catalog Number

-

Brand Name

VitreQ

Version/Model Number

FC25.R05

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

-

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

HNR

Product Code Name

Forceps, Ophthalmic

Device Record Status

Public Device Record Key

2a06f58c-b4cb-47a0-9e98-6c0efec406b3

Public Version Date

October 21, 2022

Public Version Number

1

DI Record Publish Date

October 13, 2022

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"VITREQ B.V." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 81
2 A medical device with a moderate to high risk that requires special controls. 44