FDA UDI In Commercial Distribution 🇺🇸 United States

COLABEL

DI: 10193489783872 · Model: DYNJ0365463J · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
COLABEL
Primary DI
10193489783872
Version / Model
DYNJ0365463J
Catalog Number
DYNJ0365463J
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-05-29
Public Version
1
Public Version Date
2020-06-08
Public Version Status
New
Public Device Record Key
c5cd5f9e-621e-4a2a-8ee8-8a72e17fe0b1

Device Description

CLOSUREFAST PROCEDURE PACK-LF

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
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
FDE laparoscopy kit

GMDN Terms

Code Name
10969 Intermittent venous compression system

Identifiers

Type ID
Package 40193489783873
Primary 10193489783872

Customer Contacts