FDA UDI In Commercial Distribution 🇺🇸 United States

Gyrus ACMI

DI: 00821925037960 · Model: 1010-2110-05 · Gyrus Acmi, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Gyrus ACMI
Primary DI
00821925037960
Version / Model
1010-2110-05
Company Name
Gyrus Acmi, Inc.
Labeler DUNS
007198742
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-07
Public Version
5
Public Version Date
2023-09-12
Public Version Status
Update
Public Device Record Key
ddf5282c-c42d-41e1-b80b-b2e25fa20446

Device Description

Somnoplasty Model 1010

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
44776 Electrosurgical system

Identifiers

Type ID
Package 00821925010833
Primary 00821925037960

Premarket Submissions

Submission Number Supplement Number
K971450 000