FDA UDI Not in Commercial Distribution 🇺🇸 United States

Actiwatch Spectrum Pro

DI: 00606959042032 · Model: Actiwatch Spectrum PRO Japan · Respironics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Actiwatch Spectrum Pro
Primary DI
00606959042032
Version / Model
Actiwatch Spectrum PRO Japan
Catalog Number
JP1099351
Company Name
Respironics, Inc.
Labeler DUNS
080728314
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-19
Public Version
5
Public Version Date
2021-03-05
Public Version Status
Update
Public Device Record Key
9e1b7a03-3b7e-4287-a0eb-c91678edfe05
Distribution End Date
2021-03-05

Device Description

Actiwatch Spectrum PRO Japan

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
Yes
Has Lot/Batch Number
No
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 00606959042032

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-4 – 140 Degrees Fahrenheit
Type
Storage Environment Temperature
Temperature Range
-20 – 60 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
15 – 95 Percent (%) Relative Humidity