FDA UDI In Commercial Distribution 🇺🇸 United States

Pulse Recovery Package

DI: 00817369020910 · Model: Pulse Recovery Package - Power Standard · NORMATEC INDUSTRIES LP
Product Codes
1
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Pulse Recovery Package
Primary DI
00817369020910
Version / Model
Pulse Recovery Package - Power Standard
Catalog Number
40104
Company Name
NORMATEC INDUSTRIES LP
Labeler DUNS
111448069
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-13
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
d11e6d8d-0597-4e58-84b2-b5d1b92435e1

Device Description

Pulse Recovery Package - Power Standard

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
No
Has Serial Number
Yes
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
IRP Massager, Powered Inflatable Tube

GMDN Terms

Code Name
10969 Intermittent venous compression system
16837 Sequential venous compression system

Identifiers

Type ID
Primary 00817369020910

Premarket Submissions

Submission Number Supplement Number
K160608 000