FDA UDI In Commercial Distribution 🇺🇸 United States

VOYANT® 5mm Fusion Device

DI: 00607915138424 · Model: EB210 · APPLIED MEDICAL RESOURCES CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
VOYANT® 5mm Fusion Device
Primary DI
00607915138424
Version / Model
EB210
Company Name
APPLIED MEDICAL RESOURCES CORPORATION
Labeler DUNS
187129135
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-28
Public Version
2
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
038a48ef-130a-43dc-9c5d-01e52a4e1217

Device Description

Sealer & Divider handpiece

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
Yes
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
44776 Electrosurgical system

Identifiers

Type ID
Package 10607915138421
Primary 00607915138424

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 5 Millimeter
Length 37 Centimeter