N.A. - N.A. - Geuder Aktiengesellschaft

Duns Number:316267202

Device Description: N.A.

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More Product Details

Catalog Number

38625

Brand Name

N.A.

Version/Model Number

38625

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)

-

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

HMR

Product Code Name

Marker, ocular

Device Record Status

Public Device Record Key

6fa25f30-2af3-4bb5-ba74-5fac7163a3c9

Public Version Date

March 03, 2021

Public Version Number

1

DI Record Publish Date

February 23, 2021

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"GEUDER AKTIENGESELLSCHAFT" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 504
2 A medical device with a moderate to high risk that requires special controls. 1