FDA UDI In Commercial Distribution 🇺🇸 United States

Suction Tube

DI: 10840199507372 · Model: 7219-19 · KOROS U.S.A., INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Suction Tube
Primary DI
10840199507372
Version / Model
7219-19
Catalog Number
7219-19
Company Name
KOROS U.S.A., INC.
Labeler DUNS
007928633
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-07-01
Public Version
1
Public Version Date
2022-07-11
Public Version Status
New
Public Device Record Key
067a82ea-f12b-4261-990a-f54fefb51f3b

Device Description

Fukushima-Type Tapered Large Suction 5 French 205mm Total Length

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
Yes
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
JZF Tube, Ear Suction

GMDN Terms

Code Name
38749 Surgical/emergency suction cannula, non-illuminating, reusable

Identifiers

Type ID
Direct Marking 00840199507375
Primary 10840199507372

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 9x12mm

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in dry place at room temperature