FDA UDI In Commercial Distribution 🇺🇸 United States

Med-Rx

DI: 00628725000374 · Model: 10-1040 · Canadian Hospital Specialties Limited
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Med-Rx
Primary DI
00628725000374
Version / Model
10-1040
Catalog Number
10-1040
Company Name
Canadian Hospital Specialties Limited
Labeler DUNS
240992693
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-07-17
Public Version
1
Public Version Date
2024-07-25
Public Version Status
New
Public Device Record Key
907bcbe7-2250-457e-8a70-534e559d9041

Device Description

STANDARD BORE TUBING (I.D 0.095") W/ PINCH CLAMP, M/F LL

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
FPA Set, Administration, Intravascular

GMDN Terms

Code Name
12170 Intravenous administration tubing extension set

Identifiers

Type ID
Package 50628725000379
Primary 00628725000374

Customer Contacts

Phone
9058259300