FDA UDI In Commercial Distribution 🇺🇸 United States

Solace™

DI: 04046964773105 · Model: 622517 · B BRAUN INTERVENTIONAL SYSTEMS, INC
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
Solace™
Primary DI
04046964773105
Version / Model
622517
Catalog Number
622517
Company Name
B BRAUN INTERVENTIONAL SYSTEMS, INC
Labeler DUNS
784259751
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2016-08-30
Public Version
8
Public Version Date
2022-11-02
Public Version Status
Update
Public Device Record Key
83163c8d-8827-42c6-81be-5ecc67f1d54a

Device Description

20CC-30ATM INFLATION DEVICE

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
KOE DILATOR, URETHRAL
MAV Syringe, balloon inflation

GMDN Terms

Code Name
17541 Catheter/overtube balloon inflator, single-use

Identifiers

Type ID
Primary 04046964773105
Unit of Use 04046964773099

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Capacity (ml) : 20.000 ML