FDA UDI In Commercial Distribution 🇺🇸 United States

All-Med, Inc.

DI: 10816339022029 · Model: 40-0500 · ALL-MED INC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
All-Med, Inc.
Primary DI
10816339022029
Version / Model
40-0500
Company Name
ALL-MED INC
Labeler DUNS
012789116
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
09fa6e60-2628-457f-bc44-b143a7447462

Device Description

5" Extension Set with T-Injection Site with Male luer slip with slide clamp and Female Luer Lock. Lipid Resistant, Non-DEHP PVC tubing, Latex Free. Approximate Priming Volume: .30ml

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
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
No
Has Expiration Date
No
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 10816339027987
Primary 10816339022029

Customer Contacts

Phone
603-355-4843