FDA UDI In Commercial Distribution 🇺🇸 United States

AMS Ambicor

DI: 00878953000954 · Model: 72401451 · AMERICAN MEDICAL SYSTEMS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AMS Ambicor
Primary DI
00878953000954
Version / Model
72401451
Company Name
AMERICAN MEDICAL SYSTEMS, INC.
Labeler DUNS
125111448
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-24
Public Version
5
Public Version Date
2022-04-06
Public Version Status
Update
Public Device Record Key
ff9f89db-f2a1-4a06-b05e-32d452fabfba

Device Description

Inflatable Penile Prosthesis, Prefilled and Preconnected Cylinder and Pump Component, 8 Extenders (2 each 0.5, 1, 2, 3 cm), 2 Keith Needles

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Conditional
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
FHW Device, Impotence, Mechanical/Hydraulic

GMDN Terms

Code Name
36250 Inflatable penile prosthesis

Identifiers

Type ID
Primary 00878953000954

Device Sizes

Type Value Unit Text
Lumen/Inner Diameter 12.5 Millimeter
Length 16 Centimeter