FDA UDI In Commercial Distribution 🇺🇸 United States

BIPAL

DI: 20705032054949 · Model: 502400B · CORDIS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BIPAL
Primary DI
20705032054949
Version / Model
502400B
Catalog Number
502400B
Company Name
CORDIS CORPORATION
Labeler DUNS
806136177
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-01
Public Version
6
Public Version Date
2022-09-14
Public Version Status
Update
Public Device Record Key
8c47669d-d9f8-443b-910b-b0be5bb73379

Device Description

BF BIPAL 7F 104CM 2.2MM JAW

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
DWE TUBING, PUMP, CARDIOPULMONARY BYPASS

GMDN Terms

Code Name
46679 Endomyocardial biopsy forceps, single-use

Identifiers

Type ID
Primary 20705032054949

Premarket Submissions

Submission Number Supplement Number
K933235 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius