FDA UDI In Commercial Distribution 🇺🇸 United States

AngioDynamics

DI: H787700101731M0 · Model: 700-101731M · ANGIODYNAMICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AngioDynamics
Primary DI
H787700101731M0
Version / Model
700-101731M
Company Name
ANGIODYNAMICS, INC.
Labeler DUNS
079105071
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-21
Public Version
6
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
85fd63d6-069d-4d8f-986d-3101790f19fb

Device Description

1500X RF Generator

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
35156 Percutaneous radio-frequency ablation system generator

Identifiers

Type ID
Primary H787700101731M0

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K040989 000

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
20 – 85 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-10 – 65 Degrees Celsius
Type
Handling Environment Humidity
Temperature Range
10 – 85 Percent (%) Relative Humidity
Type
Handling Environment Temperature
Temperature Range
10 – 40 Degrees Celsius