FDA UDI In Commercial Distribution 🇺🇸 United States

Actiwatch

DI: 00606959021440 · Model: Actiwatch Spectrum Plus · Respironics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Actiwatch
Primary DI
00606959021440
Version / Model
Actiwatch Spectrum Plus
Catalog Number
1101894
Company Name
Respironics, Inc.
Labeler DUNS
080728314
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-19
Public Version
4
Public Version Date
2021-02-11
Public Version Status
Update
Public Device Record Key
9f9e1922-0b1b-4dd5-ade5-2a00e8e796c9

Device Description

Actiwatch Spectrum Plus

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 00606959021440

Customer Contacts

Storage Conditions

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