FDA UDI In Commercial Distribution 🇺🇸 United States

SUMMIT MEDICAL

DI: 10385640086803 · Model: LS2000 · Summit Medical, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
12

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
SUMMIT MEDICAL
Primary DI
10385640086803
Version / Model
LS2000
Company Name
Summit Medical, Inc.
Labeler DUNS
965484699
Distribution Status
In Commercial Distribution
Device Count in Pkg
12
Record Status
Published
Publish Date
2025-07-17
Public Version
1
Public Version Date
2025-07-25
Public Version Status
New
Public Device Record Key
2e1386fd-c726-451d-af40-0e6e1a2f1d8e

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KDQ Bottle, Collection, Vacuum

GMDN Terms

Code Name
34858 Surgical suction system collection container, single-use

Identifiers

Type ID
Package 10385640086803
Primary 10385640086803
Unit of Use 00385640086806