NaturaLyte - NaturaLyte Dry Pack Sodium Bicarbonate RX 10 - Fresenius Medical Care Holdings, Inc.

Duns Number:958291411

Device Description: NaturaLyte Dry Pack Sodium Bicarbonate RX 10

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More Product Details

Catalog Number

08-4110-6

Brand Name

NaturaLyte

Version/Model Number

08-4110-6

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

KPO

Product Code Name

DIALYSATE CONCENTRATE FOR HEMODIALYSIS (LIQUID OR POWDER)

Device Record Status

Public Device Record Key

625915df-5f77-42f2-97d0-c997d46ca807

Public Version Date

November 01, 2021

Public Version Number

5

DI Record Publish Date

October 02, 2015

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"FRESENIUS MEDICAL CARE HOLDINGS, INC." Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 65