Catalog Number

5365412201

Brand Name

Celtra ®

Version/Model Number

CELTRA DUO, HT A1, C14, 1ST

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

May 06, 2022

Issuing Agency

In HIBCC

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

EIH

Product Code Name

POWDER, PORCELAIN

Public Device Record Key

c7b705eb-2472-42d1-a050-d364bd96cad3

Public Version Date

May 09, 2022

Public Version Number

2

DI Record Publish Date

September 30, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-