FDA Registration Active 🇺🇸 United States

Avaulta Plus Biosynthetic Support

Reg #: 3006082230 · FEI: 3006082230 · Expires 2025
Products
2
Proprietary Names
2
Establishment Types
1
Classifications
2

Registration Details

Registration Name
C.R. BARD, INC.
Registration Number
3006082230
FEI Number
3006082230
Status
Active
Expiry Year
2025
Initial Importer
No
Address
1211 MARY MAGNAN BLVD.
City
MADISON
State
GA
ZIP
30650
Country
US

Regulatory Submissions

510(k) Number
K063712

Owner / Operator

Firm Name
C. R. Bard, Inc.
Operator Number
2212754
Address
1 Becton Drive
City
Franklin Lakes
State
NJ
Postal Code
07417
Country
US

Products

Device Name Product Code
Mesh, Surgical, Non-Synthetic, Urogynecologic, For Pelvic Organ Prolapse, Transvaginally Placed PAI
Mesh, Surgical, Synthetic, Urogynecologic, For Pelvic Organ Prolapse, Transvaginally Placed OTP

Proprietary Names

Avaulta Plus Biosynthetic Support Avualta Solo Synthetic Support

Establishment Types

Sterilize Medical Device for Another Party (Contract Sterilizer)