FDA UDI In Commercial Distribution 🇺🇸 United States

Perclose ProGlide™

DI: 08717648013089 · Model: 12673-03 · ABBOTT VASCULAR INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Perclose ProGlide™
Primary DI
08717648013089
Version / Model
12673-03
Catalog Number
12673-03
Company Name
ABBOTT VASCULAR INC.
Labeler DUNS
964569052
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-11-21
Public Version
8
Public Version Date
2023-08-01
Public Version Status
Update
Public Device Record Key
58f9da1d-3d92-49d9-aa21-e332962717b6

Device Description

Perclose ProGlide™ Suture-Mediated Closure System

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
Yes
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
MGB DEVICE, HEMOSTASIS, VASCULAR

GMDN Terms

Code Name
52747 Femoral vessel suture implantation set

Identifiers

Type ID
Package 28717648013083
Primary 08717648013089

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry. Keep away from sunlight.