FDA UDI In Commercial Distribution 🇺🇸 United States

LaproGlide

DI: 10860009758329 · Model: U0019 · Surgical Principals, Inc
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
LaproGlide
Primary DI
10860009758329
Version / Model
U0019
Company Name
Surgical Principals, Inc
Labeler DUNS
782873892
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2024-05-20
Public Version
1
Public Version Date
2024-05-28
Public Version Status
New
Public Device Record Key
f7118d07-a5a6-4e29-b654-7165c22a6196

Device Description

Laparoscopic Curved Blade Electrode, 33cm Length, PTFE

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
Yes
Has Expiration Date
Yes
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
61874 Open-surgery electrosurgical electrode, monopolar, single-use

Identifiers

Type ID
Unit of Use 00860009758322
Primary 10860009758329