FDA UDI In Commercial Distribution 🇺🇸 United States

SafeDAY™

DI: 04046964293177 · Model: 352241 · B. BRAUN MEDICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
50

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Basic Information

Brand Name
SafeDAY™
Primary DI
04046964293177
Version / Model
352241
Catalog Number
352241
Company Name
B. BRAUN MEDICAL INC.
Labeler DUNS
002397347
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2016-09-23
Public Version
4
Public Version Date
2021-04-07
Public Version Status
Update
Public Device Record Key
707980c1-4ff4-4681-b537-3eb808952283

Device Description

10 DR SAFEDAY SET W/PORTS, 2 SAFEDAY VLV

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
58977 Basic intravenous administration set, noninvasive

Identifiers

Type ID
Primary 04046964293177
Unit of Use 04046964293160

Customer Contacts