FDA UDI In Commercial Distribution 🇺🇸 United States

Gyrus ACMI

DI: 00821925041677 · Model: 1200-2110-05 · Gyrus Acmi, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Gyrus ACMI
Primary DI
00821925041677
Version / Model
1200-2110-05
Company Name
Gyrus Acmi, Inc.
Labeler DUNS
007198742
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-28
Public Version
6
Public Version Date
2023-09-14
Public Version Status
Update
Public Device Record Key
1001f72b-8f28-4ad4-a6a0-ed073f19aec2

Device Description

Somnoplasty Model 1200

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
44776 Electrosurgical system

Identifiers

Type ID
Package 00821925010147
Primary 00821925041677

Premarket Submissions

Submission Number Supplement Number
K982717 000