FDA UDI In Commercial Distribution 🇺🇸 United States

GYRUS ACMI, INC

DI: 00821925016392 · Model: 131010 · Gyrus Acmi, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
GYRUS ACMI, INC
Primary DI
00821925016392
Version / Model
131010
Company Name
Gyrus Acmi, Inc.
Labeler DUNS
007198742
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-10
Public Version
3
Public Version Date
2023-10-19
Public Version Status
Update
Public Device Record Key
96450601-c152-4836-b690-799395b1edf3

Device Description

ALLIGATOR FORCEPS, STRAIGHT, SERRATED

Device Characteristics

Single Use
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
LRC INSTRUMENT, ENT MANUAL SURGICAL

GMDN Terms

Code Name
39987 Nasal depth gauge, reusable

Identifiers

Type ID
Primary 00821925016392