FDA UDI In Commercial Distribution 🇺🇸 United States

Checkpoint Gemini

DI: B13090920 · Model: 9092 · Checkpoint Surgical, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
1

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Basic Information

Brand Name
Checkpoint Gemini
Primary DI
B13090920
Version / Model
9092
Catalog Number
9092
Company Name
Checkpoint Surgical, Inc.
Labeler DUNS
832575364
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-03-30
Public Version
1
Public Version Date
2022-04-07
Public Version Status
New
Public Device Record Key
d83b782d-24f7-4d43-b9d5-528da7a6b1d4

Device Description

Handheld Single-use Surgical Bipolar Nerve Stimulator

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
ETN Stimulator, Nerve

GMDN Terms

Code Name
35723 Nerve-locating system

Identifiers

Type ID
Package B13090921
Primary B13090920
Package B13090922
Package B13090923

Customer Contacts

Phone
216-378-9107

Premarket Submissions

Submission Number Supplement Number
K092292 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-20 – 55 Degrees Celsius