FDA UDI In Commercial Distribution 🇺🇸 United States

DOUBLEFLO

DI: 03661379195499 · Model: A · HEMODIA
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
30

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Basic Information

Brand Name
DOUBLEFLO
Primary DI
03661379195499
Version / Model
A
Catalog Number
72205353
Company Name
HEMODIA
Labeler DUNS
381957786
Distribution Status
In Commercial Distribution
Device Count in Pkg
30
Record Status
Published
Publish Date
2021-04-13
Public Version
1
Public Version Date
2021-04-21
Public Version Status
New
Public Device Record Key
dd0ce1fc-ad74-4e92-9297-a58d492f072a

Device Description

DOUBLEFLO DAY TUBE SET

Device Characteristics

Single Use
No
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
HRX Arthroscope

GMDN Terms

Code Name
47625 Surgical irrigation/aspiration tubing set

Identifiers

Type ID
Unit of Use 23661379195493
Primary 03661379195499

Premarket Submissions

Submission Number Supplement Number
K203480 000