FDA UDI In Commercial Distribution 🇺🇸 United States

INTERLINK

DI: 00085412013619 · Model: 1C8333 · BAXTER INTERNATIONAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
INTERLINK
Primary DI
00085412013619
Version / Model
1C8333
Catalog Number
1C8333
Company Name
BAXTER INTERNATIONAL INC.
Labeler DUNS
005146311
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
7
Public Version Date
2021-03-08
Public Version Status
Update
Public Device Record Key
8a83997c-db37-4bce-920f-dcf0d27cd17f

Device Description

Blood Bag Spike, Injection Site

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
Yes
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
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FPA Set, administration, intravascular

GMDN Terms

Code Name
38569 Blood transfusion set, non-exchange

Identifiers

Type ID
Package 50085412013614
Primary 00085412013619

Customer Contacts