FDA UDI In Commercial Distribution 🇺🇸 United States

SafeDAY™

DI: 04046964293238 · Model: 352244 · B. BRAUN MEDICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
100

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Basic Information

Brand Name
SafeDAY™
Primary DI
04046964293238
Version / Model
352244
Catalog Number
352244
Company Name
B. BRAUN MEDICAL INC.
Labeler DUNS
002397347
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2016-09-23
Public Version
3
Public Version Date
2018-08-29
Public Version Status
Update
Public Device Record Key
a05d6de1-64e3-41df-a74a-6568f10b6263

Device Description

SAFEDAY EXTENSION SET W/ SPIN-LOCK 8 in.

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FPA Set, administration, intravascular

GMDN Terms

Code Name
12170 Intravenous administration tubing extension set

Identifiers

Type ID
Primary 04046964293238
Unit of Use 04046964293221

Customer Contacts