FDA UDI In Commercial Distribution 🇺🇸 United States

Aquamantys™

DI: 00763000738495 · Model: 23-313-1 · MEDTRONIC NAVIGATION, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Aquamantys™
Primary DI
00763000738495
Version / Model
23-313-1
Company Name
MEDTRONIC NAVIGATION, INC.
Labeler DUNS
835233107
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-03-24
Public Version
1
Public Version Date
2025-04-01
Public Version Status
New
Public Device Record Key
01a84e36-babc-4f06-bc98-6d09ae9df034

Device Description

AQUAMANTYS 9.5 XL BIPOLAR SEALER DEVICE

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 00763000738495

Customer Contacts