FDA UDI In Commercial Distribution 🇺🇸 United States

Aquamantys®

DI: 00643169078338 · Model: 40-402-1R · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Aquamantys®
Primary DI
00643169078338
Version / Model
40-402-1R
Company Name
MEDTRONIC, INC.
Labeler DUNS
030200852
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-25
Public Version
3
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
7cf7ab9c-bff2-4abd-b142-ee98e41d5ff8

Device Description

GENERATOR 40-402-1R REFURB AQM 115V

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
No
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
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

GMDN Terms

Code Name
11490 Electrosurgical system generator

Identifiers

Type ID
Primary 00643169078338

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
14 – 149 Degrees Fahrenheit
Type
Storage Environment Humidity
Temperature Range
0 – 95 Percent (%) Relative Humidity