FDA UDI In Commercial Distribution 🇺🇸 United States

Lasso

DI: 00816734023037 · Model: 1180-13 · DIVERSATEK HEALTHCARE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Lasso
Primary DI
00816734023037
Version / Model
1180-13
Company Name
DIVERSATEK HEALTHCARE, INC.
Labeler DUNS
030650113
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-02-26
Public Version
1
Public Version Date
2021-03-08
Public Version Status
New
Public Device Record Key
4f7984bd-52b2-4ef3-8526-e9e71c98b2f1

Device Description

Lasso Polypectomy Snare

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
Yes
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
No

Product Codes

Code Name
FGX Snare, Non-Electrical

GMDN Terms

Code Name
62615 Mechanical-cutting endoscopic polypectomy snare

Identifiers

Type ID
Package 10816734023034
Primary 00816734023037
Package 20816734023031

Customer Contacts

Phone
800-558-6408

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry
Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight
Type
Storage Environment Temperature
Temperature Range
-10 – 40 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
30 – 80 Percent (%) Relative Humidity
Type
Storage Environment Atmospheric Pressure
Temperature Range
86 – 106 KiloPascal