FDA UDI Not in Commercial Distribution 🇺🇸 United States

LTX Pk w/Ped Hardshell Reser

DI: 00607567203679 · Model: BO-TOP 23406 · DATASCOPE CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LTX Pk w/Ped Hardshell Reser
Primary DI
00607567203679
Version / Model
BO-TOP 23406
Catalog Number
701055221
Company Name
DATASCOPE CORP.
Labeler DUNS
001660786
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-01-08
Public Version
6
Public Version Date
2022-12-08
Public Version Status
Update
Public Device Record Key
e5be0fbf-bda4-4422-99c4-94707fe79dd1
Distribution End Date
2018-07-20

Device Description

HMO 70000 BO-VHK 31000 Blood Transfer Bag BO-RF32 Pall LG6 Arterial Filter Gas Filter

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
Yes
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
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

GMDN Terms

Code Name
35441 Cardiopulmonary bypass system blood tubing set

Identifiers

Type ID
Primary 00607567203679

Customer Contacts

Phone
18886278383

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
10 – 30 Degrees Celsius