FDA UDI In Commercial Distribution 🇺🇸 United States

HydroMID

DI: 00850030354426 · Model: MID-251 · Access Vascular, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HydroMID
Primary DI
00850030354426
Version / Model
MID-251
Company Name
Access Vascular, Inc.
Labeler DUNS
085539114
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-11-18
Public Version
1
Public Version Date
2025-11-26
Public Version Status
New
Public Device Record Key
1b6c3997-5477-4650-a592-9e08014c24f4

Device Description

HydroMID 5Fr Dual Lumen Marked catheter

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
MR Conditional
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
FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

GMDN Terms

Code Name
36257 Peripherally-inserted central venous catheter

Identifiers

Type ID
Primary 00850030354426