FDA UDI In Commercial Distribution 🇺🇸 United States

Respiguide Delivery System

DI: 00857688007278 · Model: 7120-S · RESPICARDIA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Respiguide Delivery System
Primary DI
00857688007278
Version / Model
7120-S
Company Name
RESPICARDIA, INC.
Labeler DUNS
027887663
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-04-30
Public Version
6
Public Version Date
2021-12-22
Public Version Status
Update
Public Device Record Key
a6c4b55a-db17-4454-8985-8b620a0aced8

Device Description

Respiguide Delivery System, 35 cm Outer Guide Catheter with 120 degree bend Distal shape; 65 cm Inner Angiographic Catheter with Straight Distal Shape

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
No
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DQO Catheter, Intravascular, Diagnostic

GMDN Terms

Code Name
17846 Vascular guide-catheter, single-use

Identifiers

Type ID
Primary 00857688007278
Package 10857688007275

Customer Contacts

Phone
+19525404471

Premarket Submissions

Submission Number Supplement Number
K130378 000