FDA UDI In Commercial Distribution 🇺🇸 United States

USA Elite

DI: 00821925001237 · Model: E8213 · Gyrus ACMI, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
USA Elite
Primary DI
00821925001237
Version / Model
E8213
Company Name
Gyrus ACMI, LLC
Labeler DUNS
007198742
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-13
Public Version
3
Public Version Date
2024-09-02
Public Version Status
Update
Public Device Record Key
9ee2a04e-5b2f-4cce-a6b9-8bcae1a25e6d

Device Description

USA Elite System Rigid Optical Cup Tearing Biopsy Forceps

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
Yes
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
GEN FORCEPS, GENERAL & PLASTIC SURGERY

GMDN Terms

Code Name
35732 Rigid endoscopic biopsy forceps, reusable

Identifiers

Type ID
Primary 00821925001237