FDA UDI In Commercial Distribution 🇺🇸 United States

InjecSURE ®

DI: 00850002461404 · Model: 890-305SS · Carbon Medical Technologies, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
InjecSURE ®
Primary DI
00850002461404
Version / Model
890-305SS
Catalog Number
890-305SS
Company Name
Carbon Medical Technologies, Inc.
Labeler DUNS
883094039
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-04-09
Public Version
1
Public Version Date
2026-04-17
Public Version Status
New
Public Device Record Key
32b4c9c7-6e0a-488c-a8fb-d17a6cc5395b

Device Description

Injection 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
Yes
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
FBK Endoscopic Injection Needle, Gastroenterology-Urology

GMDN Terms

Code Name
38825 General-purpose endoscopic needle, single-use

Identifiers

Type ID
Package 10850002461401
Primary 00850002461404

Customer Contacts

Phone
6516538512

Device Sizes

Type Value Unit Text
Needle Gauge 20 Gauge
Length 127 Millimeter
Length 5 Inch
Device Size Text, specify Spinal