FDA UDI In Commercial Distribution 🇺🇸 United States

Retention Cuff Inflator

DI: 10815112020887 · Model: 900405 · BRACCO DIAGNOSTICS INC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
12

Basic Information

Brand Name
Retention Cuff Inflator
Primary DI
10815112020887
Version / Model
900405
Catalog Number
900405
Company Name
BRACCO DIAGNOSTICS INC
Labeler DUNS
849234661
Distribution Status
In Commercial Distribution
Device Count in Pkg
12
Record Status
Published
Publish Date
2016-09-19
Public Version
3
Public Version Date
2020-06-30
Public Version Status
Update
Public Device Record Key
53b0064c-8c28-4b8c-a225-73a3f94754c5

Device Description

One Shot Cuff Inflator

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FGD Catheter, Retention, Barium Enema With Bag

GMDN Terms

Code Name
34912 Barium enema catheter

Identifiers

Type ID
Package 30815112020881
Primary 10815112020887
Unit of Use 00815112020880

Customer Contacts

Phone
609-514-2200