FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 00085412003252 · Model: 2B8066 · BAXTER INTERNATIONAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
300

Basic Information

Brand Name
N/A
Primary DI
00085412003252
Version / Model
2B8066
Catalog Number
2B8066
Company Name
BAXTER INTERNATIONAL INC.
Labeler DUNS
005146311
Distribution Status
In Commercial Distribution
Device Count in Pkg
300
Record Status
Published
Publish Date
2016-09-24
Public Version
4
Public Version Date
2019-10-23
Public Version Status
Update
Public Device Record Key
8020d8a1-7506-4e96-886c-715bd0cd82a3

Device Description

Additive Cap

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
No
Sterilization Prior Use
No

Product Codes

Code Name
KPE CONTAINER, I.V.

GMDN Terms

Code Name
35127 Intravenous administration bag/bottle

Identifiers

Type ID
Package 50085412003257
Primary 00085412003252
Unit of Use 70085412003251

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K111217 000