FDA UDI Not in Commercial Distribution 🇺🇸 United States

Aquamantys ®3

DI: 00643169465985 · Model: 23-318-1 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Aquamantys ®3
Primary DI
00643169465985
Version / Model
23-318-1
Company Name
MEDTRONIC, INC.
Labeler DUNS
030200852
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-16
Public Version
3
Public Version Date
2019-03-12
Public Version Status
Update
Public Device Record Key
6c361c28-149c-4968-a7f9-d6e6b6e8560a
Distribution End Date
2017-06-27

Device Description

BIPO SEALER 23-318-1 AQM3 DBS 8.7 ROHS

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 00643169465985

Customer Contacts

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
15 – 85 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
50 – 104 Degrees Fahrenheit