FDA UDI In Commercial Distribution 🇺🇸 United States

Hose

DI: 08809802640672 · Model: 1000370 · DAESUNG MAREF CO.,LTD.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

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Basic Information

Brand Name
Hose
Primary DI
08809802640672
Version / Model
1000370
Company Name
DAESUNG MAREF CO.,LTD.
Labeler DUNS
688817949
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-12-17
Public Version
1
Public Version Date
2021-12-27
Public Version Status
New
Public Device Record Key
e7a25d55-11e4-4216-afb9-42a940a3b8c6

Device Description

Single Hose 2m 1ea [One polybag]

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
Yes
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IRP Massager, Powered Inflatable Tube

GMDN Terms

Code Name
10969 Intermittent venous compression system

Identifiers

Type ID
Package 18809802640679
Primary 08809802640672
Package 28809802640676

Premarket Submissions

Submission Number Supplement Number
K202395 000
K203019 000
K203498 000