FDA UDI In Commercial Distribution 🇺🇸 United States

VENTRALIGHT

DI: 00801741031663 · Model: 5954790 · Davol Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
VENTRALIGHT
Primary DI
00801741031663
Version / Model
5954790
Catalog Number
5954790
Company Name
Davol Inc.
Labeler DUNS
001191048
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-05-17
Public Version
5
Public Version Date
2024-10-22
Public Version Status
Update
Public Device Record Key
4512cb38-6079-4b22-bd92-1b03b1d75448

Device Description

Ventralight ST Mesh, 7" x 9" (17.8 cm x 22.9 cm), Ellipse

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
FTL Mesh, surgical, polymeric

GMDN Terms

Code Name
44756 Extra-gynaecological surgical mesh, composite-polymer

Identifiers

Type ID
Primary 00801741031663

Customer Contacts

Device Sizes

Type Value Unit Text
Length 22.9 Centimeter
Width 17.8 Centimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 25 Degrees Celsius