FDA UDI In Commercial Distribution 🇺🇸 United States

K-Pack II

DI: 05413206032037 · Model: KN-2232RB · Terumo Europe NV
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
K-Pack II
Primary DI
05413206032037
Version / Model
KN-2232RB
Catalog Number
KN-2232RB
Company Name
Terumo Europe NV
Labeler DUNS
370193559
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-05
Public Version
6
Public Version Date
2022-10-28
Public Version Status
Update
Public Device Record Key
359b8f98-5ca2-4aef-a3dc-4377ff6b0c3e

Device Description

K-Pack II Needle

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
FMI Needle, Hypodermic, Single Lumen

GMDN Terms

Code Name
59230 Hypodermic needle, single-use

Identifiers

Type ID
Primary 05413206032037
Package 55413206032032

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K984576 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Needle Length: 1.25 Inch
Needle Gauge 22 Gauge
Device Size Text, specify Needle Length: 30 Millimeter
Device Size Text, specify Needle Outer Diameter: 0.7 Millimeter
Device Size Text, specify Thin wall

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight. Keep dry.
Type
Storage Environment Temperature
Temperature Range
2 – 30 Degrees Celsius