FDA UDI In Commercial Distribution 🇺🇸 United States

Aquamantys ™

DI: 00763000058678 · Model: 23-321-1 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Aquamantys ™
Primary DI
00763000058678
Version / Model
23-321-1
Company Name
MEDTRONIC, INC.
Labeler DUNS
030200852
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-07-12
Public Version
1
Public Version Date
2018-08-13
Public Version Status
New
Public Device Record Key
b5edc455-7e71-4670-8189-e48e92765210

Device Description

BIPO SEALER 23-321-1 AQM MIS FLEX

Device Characteristics

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GEI Electrosurgical, cutting & coagulation & accessories

GMDN Terms

Code Name
56296 Open-surgery electrosurgical handpiece/electrode, bipolar, single-use

Identifiers

Type ID
Primary 00763000058678

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
50 – 104 Degrees Fahrenheit
Type
Storage Environment Temperature
Temperature Range
10 – 40 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
0 – 85 Percent (%) Relative Humidity