FDA UDI In Commercial Distribution 🇺🇸 United States

Angiography Drape Pack Fistulagram

DI: 00886333212910 · Model: 401035A · ARGON MEDICAL DEVICES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Angiography Drape Pack Fistulagram
Primary DI
00886333212910
Version / Model
401035A
Catalog Number
401035A
Company Name
ARGON MEDICAL DEVICES, INC.
Labeler DUNS
140727624
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-15
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
ea1a33a7-b9e1-473e-8c2a-75cc899f4c47

Device Description

Angiography Drape Pack Fistulagram

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KKX Drape, Surgical

GMDN Terms

Code Name
16006 Angiographic drape

Identifiers

Type ID
Package 20886333212914
Primary 00886333212910

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 40" x 60"