Catalog Number

-

Brand Name

Albahealth

Version/Model Number

BLF700012100304

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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"

Yes

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

K123308,K123308

Product Code

JOW

Product Code Name

SLEEVE, LIMB, COMPRESSIBLE

Public Device Record Key

d386765b-6e06-402e-82cd-1b23f2e85b0e

Public Version Date

March 11, 2019

Public Version Number

1

DI Record Publish Date

March 01, 2019

Package DI Number

50073614776840

Quantity per Package

24

Contains DI Package

00073614776845

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-