FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 04037691730660 · Model: PIK 100 · Maquet Cardiopulmonary AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
04037691730660
Version / Model
PIK 100
Catalog Number
70105.3068
Company Name
Maquet Cardiopulmonary AG
Labeler DUNS
316153865
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-11-04
Public Version
4
Public Version Date
2019-06-07
Public Version Status
Update
Public Device Record Key
d6b12859-568c-4f24-a4cf-f73f195e6894

Device Description

Percutaneous Insertion Kit 100

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
DWF CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS

GMDN Terms

Code Name
58865 Vascular catheter introduction set, nonimplantable

Identifiers

Type ID
Primary 04037691730660

Customer Contacts

Phone
+49072229320

Premarket Submissions

Submission Number Supplement Number
K131666 000

Device Sizes

Type Value Unit Text
Device Size Text, specify OD dilator 10/12 French
Device Size Text, specify OD dilator 14/16 French
Device Size Text, specify OD puncture needle 18 Gauge
Device Size Text, specify OD Guidewire 0.038 Inch
Device Size Text, specify OD dilator 16/18 French
Device Size Text, specify OD dilator 12/14 French
Device Size Text, specify Syringe 10 Milliliter
Device Size Text, specify Guidewire length 100 Centimeter