FDA UDI Not in Commercial Distribution 🇺🇸 United States

Alyte™ Y-Mesh Graft

DI: 00801741016165 · Model: Y500 · C. R. Bard, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Alyte™ Y-Mesh Graft
Primary DI
00801741016165
Version / Model
Y500
Catalog Number
Y500
Company Name
C. R. Bard, Inc.
Labeler DUNS
016898496
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-14
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
8ad752f1-a241-4c72-964c-ab26307ef2ba
Distribution End Date
2016-12-31

Device Description

Alyte™ Y-Mesh Graft, 5 Pack

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
OTO Mesh, surgical, synthetic, urogynecologic, for apical vaginal and uterine prolapse, transabdominally placed

GMDN Terms

Code Name
60842 Pelvic organ prolapse surgical mesh, synthetic polymer

Identifiers

Type ID
Package 10801741016162
Primary 00801741016165

Customer Contacts