FDA UDI Not in Commercial Distribution 🇺🇸 United States

Aleve

DI: 00325866564948 · Model: 1613579 · BAYER HEALTHCARE LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

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Basic Information

Brand Name
Aleve
Primary DI
00325866564948
Version / Model
1613579
Company Name
BAYER HEALTHCARE LLC
Labeler DUNS
112117283
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-01
Public Version
4
Public Version Date
2019-10-23
Public Version Status
Update
Public Device Record Key
98aaee1b-904b-4407-9b03-0c3b4a1368d7
Distribution End Date
2019-02-26

Device Description

2 pairs of Aleve Direct Therapy TENs Device Refill Gel Pads packaged in one re-sealable pouch.

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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter

GMDN Terms

Code Name
35372 Analgesic transcutaneous electrical nerve stimulation system

Identifiers

Type ID
Primary 00325866564948
Package 10325866564945
Package 10325866572445

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 85 Degrees Fahrenheit
Type
Handling Environment Temperature
Temperature Range
-4 – Degrees Fahrenheit
Type
Handling Environment Temperature
Temperature Range
– 149 Degrees Fahrenheit