FDA UDI In Commercial Distribution 🇺🇸 United States

KBMED

DI: 20810100051253 · Model: SBCNP25K-1 · KB Medical (group), Inc.
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

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Basic Information

Brand Name
KBMED
Primary DI
20810100051253
Version / Model
SBCNP25K-1
Company Name
KB Medical (group), Inc.
Labeler DUNS
105002071
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-05-21
Public Version
1
Public Version Date
2025-05-29
Public Version Status
New
Public Device Record Key
f0fd08f2-68d7-4f83-90cf-8d3c95034227

Device Description

PUSH BUTTON SAFETY BLOOD COLLECTION SET, 25G*3/4" with 12" tubing, case of 200pcs

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
Yes
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FPA Set, Administration, Intravascular
JKA Tubes, Vials, Systems, Serum Separators, Blood Collection

GMDN Terms

Code Name
58497 Blood collection set, invasive

Identifiers

Type ID
Package 30810100051250
Primary 20810100051253
Unit of Use 00810100051259