FDA UDI In Commercial Distribution 🇺🇸 United States

LaparoLight

DI: 20845854061364 · Model: LLVN15012 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
12

Basic Information

Brand Name
LaparoLight
Primary DI
20845854061364
Version / Model
LLVN15012
Catalog Number
LLVN15012
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
12
Record Status
Published
Publish Date
2020-12-07
Public Version
1
Public Version Date
2020-12-15
Public Version Status
New
Public Device Record Key
d760332e-909f-4b48-906c-81e2057a16c2

Device Description

LaparoLight Veress Needle

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
HIF Insufflator, laparoscopic

GMDN Terms

Code Name
12750 Spring-loaded pneumoperitoneum needle, single-use

Identifiers

Type ID
Package 30845854061361
Primary 20845854061364
Unit of Use 00845854061360

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K171139 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 150 mm

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep Dry