FDA UDI In Commercial Distribution 🇺🇸 United States

Actical Software

DI: 00606959021013 · Model: 3.11 · Respironics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Actical Software
Primary DI
00606959021013
Version / Model
3.11
Catalog Number
1081738
Company Name
Respironics, Inc.
Labeler DUNS
080728314
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-21
Public Version
3
Public Version Date
2020-03-05
Public Version Status
Update
Public Device Record Key
f8be46a8-3070-4780-b48b-8b7fdb9308d6
Distribution End Date
9999-12-31

Device Description

Actical Software Global

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IKK SYSTEM, ISOKINETIC TESTING AND EVALUATION

GMDN Terms

Code Name
36252 Kinesiology ambulatory recorder

Identifiers

Type ID
Primary 00606959021013

Customer Contacts