FDA UDI In Commercial Distribution 🇺🇸 United States

VENTRALIGHT

DI: 00801741131035 · Model: 5990020 · Davol Inc.
Product Codes
3
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
VENTRALIGHT
Primary DI
00801741131035
Version / Model
5990020
Catalog Number
5990020
Company Name
Davol Inc.
Labeler DUNS
001191048
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-08-25
Public Version
6
Public Version Date
2024-10-22
Public Version Status
Update
Public Device Record Key
f87d4d14-bd11-4c50-9f15-51d0e99d26ab

Device Description

Ventralight ST Mesh with Echo 2 Positioning System, 8" (20 cm), Circle

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
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GCJ Laparoscope, general & plastic surgery
ORQ Mesh, surgical, deployer
FTL Mesh, surgical, polymeric

GMDN Terms

Code Name
44756 Extra-gynaecological surgical mesh, composite-polymer
61372 Surgical mesh laparoscopic delivery/positioning device

Identifiers

Type ID
Primary 00801741131035

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 20 Centimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 25 Degrees Celsius