FDA UDI In Commercial Distribution 🇺🇸 United States

Coblation

DI: 00817470002096 · Model: EIC4855-01 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Coblation
Primary DI
00817470002096
Version / Model
EIC4855-01
Catalog Number
EIC4855-01
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-29
Public Version
5
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
f9305361-0ac9-4dd6-9abb-5851b4cfe35a

Device Description

ENT COBLATOR II, REFLEX ULTRA 55 WITH INTEGRATED CABLE

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
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
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

GMDN Terms

Code Name
57944 Endoscopic electrosurgical handpiece/electrode, bipolar, single-use

Identifiers

Type ID
Primary 00817470002096

Customer Contacts