POLYFLUX REVACLEAR

Primary DI
37332414101696
Brand
POLYFLUX REVACLEAR
Company
GAMBRO RENAL PRODUCTS, INC.
Model
110633
Catalog number
110633
Device description
Revaclear-Revaclear Max are indicated for the treatment of chronic and acute renal failure by hemodialysis
Published
2015-10-07
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
KDIDialyzer, high permeability with or without sealed dialysate system

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KDIDialyzer, High Permeability With Or Without Sealed Dialysate SystemGastroenterology, Urology2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K072232000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K072232000GAMBRO POLYFLUX HEMODIALYZER, MODEL: HD-C4 SMALLGambro Renal Products, Inc.2007-09-07KDI

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
37332414101696PackageGS124In Commercial Distribution
07332414101695PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
3733241410169637332414101696
07332414101695073324141016957332414101695

GMDN Terms#

Term, Definition table
TermDefinition
Hollow-fibre haemodialysis dialyser, single-useA filter that functions as an artificial kidney and typically used in a haemodialysis system to remove impurities/fluid from the blood of a patient. It typically consists of cylindrical containers with thousands of longitudinally arranged hollow-fibre capillary tubes (e.g., polymer, modified cellulose) through which the blood flows. The tube walls function as a semi-permeable membrane, permitting passage of larger molecules from the blood to the dialysate on the outside of the tubes for removal. This is a single-use device.

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Handling Environment Temperature030 Degrees Celsius
Handling Environment Temperature0 Degrees Celsius30 Degrees Celsius

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+1(800)933-0303Medinfo_medproducts@baxter.com

Regulatory Flags#

DUNS number
929768682
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
07332414123055REVACLEAR300114745L2017-02-08
07332414124076REVACLEAR400114746L2018-01-15
07332414101695POLYFLUX REVACLEAR1106331106332015-10-07
07332414101701POLYFLUX REVACLEAR MAX1106341106342015-10-07
37332414101702POLYFLUX REVACLEAR MAX1106341106342015-10-07
37332414123056REVACLEAR300114745L2017-02-08
37332414124077REVACLEAR400114746L2018-01-15

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