FDA UDI In Commercial Distribution 🇺🇸 United States

Alaris

DI: 07613203011112 · Model: 30822 · BD Switzerland Sàrl
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Alaris
Primary DI
07613203011112
Version / Model
30822
Catalog Number
30822
Company Name
BD Switzerland Sàrl
Labeler DUNS
482631558
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-22
Public Version
5
Public Version Date
2024-03-06
Public Version Status
Update
Public Device Record Key
207d4aee-7c8e-4a76-853f-57b14cb15978

Device Description

Extension Set, 157 cm (62 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 07613203011112
Package 37613203011120

Customer Contacts

Device Sizes

Type Value Unit Text
Length 62 Inch

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-40 – 125 Degrees Fahrenheit