FDA UDI In Commercial Distribution 🇺🇸 United States

GYRUS ACMI, INC

DI: 00821925036178 · Model: 920005PK · Gyrus Acmi, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
GYRUS ACMI, INC
Primary DI
00821925036178
Version / Model
920005PK
Company Name
Gyrus Acmi, Inc.
Labeler DUNS
007198742
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-12
Public Version
5
Public Version Date
2023-08-14
Public Version Status
Update
Public Device Record Key
48f22e33-f5cb-4516-8bfd-2577561e3c47

Device Description

PKS Cutting Forceps 5mm/33cm

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
Package 00821925010352
Primary 00821925036178

Premarket Submissions

Submission Number Supplement Number
K023492 000