FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10886704067764 · Model: 60-2950US · Medos International Sàrl
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10886704067764
Version / Model
60-2950US
Catalog Number
602950US
Company Name
Medos International Sàrl
Labeler DUNS
482661753
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-20
Public Version
4
Public Version Date
2022-01-28
Public Version Status
Update
Public Device Record Key
9a460647-ec39-4b30-8d04-e912c8794b53
Distribution End Date
2024-12-31

Device Description

Intraspinal Catheter Connector with Strain Relief Sleeve

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
LKK PUMP, INFUSION, IMPLANTED, PROGRAMMABLE

GMDN Terms

Code Name
61493 Spinal port/catheter

Identifiers

Type ID
Primary 10886704067764

Customer Contacts

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
15 – 25 Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
15 – 25 Degrees Celsius
Type
Handling Environment Temperature
Temperature Range
59 – 77 Degrees Fahrenheit
Type
Storage Environment Temperature
Temperature Range
59 – 77 Degrees Fahrenheit
Type
Special Storage Condition, Specify
Special Conditions
Do not use if opened or damaged.