FDA UDI In Commercial Distribution 🇺🇸 United States

Vilet™

DI: 10841307130604 · Model: V392U · IMPLANT DIRECT SYBRON MANUFACTURING LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Vilet™
Primary DI
10841307130604
Version / Model
V392U
Catalog Number
V392U
Company Name
IMPLANT DIRECT SYBRON MANUFACTURING LLC
Labeler DUNS
868856969
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-16
Public Version
6
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
8ade6256-0545-4bf4-9176-55fbfbafda77

Device Description

Vilet PGLA 4/0 FS-2 [3/8C RevCt 19mm] 18” Undyed

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GAM Suture, Absorbable, Synthetic, Polyglycolic Acid

GMDN Terms

Code Name
17471 Polyester suture, bioabsorbable, multifilament, non-antimicrobial

Identifiers

Type ID
Package 20841307130601
Primary 10841307130604

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K120556 000

Device Sizes

Type Value Unit Text
Device Size Text, specify USP: 4-0 Length: 18in.