FDA UDI In Commercial Distribution 🇺🇸 United States

BEAMER

DI: 10653405986461 · Model: S-BEAM-3 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
BEAMER
Primary DI
10653405986461
Version / Model
S-BEAM-3
Catalog Number
S-BEAM-3
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2019-04-15
Public Version
2
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
593deb22-040d-4380-b8ef-efd9f737de5b

Device Description

BEAMER ARGON SIDEFIRE PROBE, SIDEFIRE PROBE FOR FLEXIBLE ENDOSCOPY

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GEI Electrosurgical, cutting & coagulation & accessories

GMDN Terms

Code Name
61878 Inert gas-enhanced endoscopic electrosurgical electrode, single-use

Identifiers

Type ID
Package 20653405986468
Primary 10653405986461
Unit of Use 00653405986464

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K081644 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 2.3 mm x 320 cm

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
KEEP DRY