FDA UDI In Commercial Distribution 🇺🇸 United States

Endoplus

DI: 00817401026412 · Model: E310MR · Endoplus
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Endoplus
Primary DI
00817401026412
Version / Model
E310MR
Company Name
Endoplus
Labeler DUNS
794679167
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-01-08
Public Version
4
Public Version Date
2019-08-21
Public Version Status
Update
Public Device Record Key
dc91e2a5-4b23-44f1-829c-542b51687232

Device Description

5mm Round Tip Allis Grasping Forcep, Monopolar Handle, With Rotation

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

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HFI Coagulator, Culdoscopic (And Accessories)

GMDN Terms

Code Name
35080 Rigid endoscopic tissue manipulation forceps, reusable

Identifiers

Type ID
Primary 00817401026412

Premarket Submissions

Submission Number Supplement Number
K925079 000