FDA UDI In Commercial Distribution 🇺🇸 United States

Endoplus

DI: 00817401024760 · Model: E348SLR-45 · Endoplus
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Endoplus
Primary DI
00817401024760
Version / Model
E348SLR-45
Company Name
Endoplus
Labeler DUNS
794679167
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-31
Public Version
4
Public Version Date
2019-08-21
Public Version Status
Update
Public Device Record Key
d3554558-71d0-4f33-9c88-5a2edbe101df

Device Description

5mm Ripple Claw Forcep, Slide Lock Handle, With Rotation, 45cm

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
HET Laparoscope, Gynecologic (And Accessories)

GMDN Terms

Code Name
35080 Rigid endoscopic tissue manipulation forceps, reusable

Identifiers

Type ID
Primary 00817401024760

Premarket Submissions

Submission Number Supplement Number
K925079 000