FDA UDI In Commercial Distribution 🇺🇸 United States

POD Active Knee Brace

DI: 09344006000819 · Model: K8 2.0 (Pairs) · POD ACTIVE PTY LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
POD Active Knee Brace
Primary DI
09344006000819
Version / Model
K8 2.0 (Pairs)
Company Name
POD ACTIVE PTY LTD
Labeler DUNS
759177843
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-04-29
Public Version
3
Public Version Date
2022-08-30
Public Version Status
Update
Public Device Record Key
70379ad6-e3e7-439d-9bb2-7774e70c1c87

Device Description

POD Active Knee Brace; model K8; version 2.0; pairs (LT & RT)

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
ITQ Joint, Knee, External Brace

GMDN Terms

Code Name
41065 Knee support orthosis

Identifiers

Type ID
Primary 09344006000819

Customer Contacts

Phone
+61352444111

Device Sizes

Type Value Unit Text
Device Size Text, specify SM
Device Size Text, specify MD
Device Size Text, specify LG
Device Size Text, specify XL