FDA UDI Not in Commercial Distribution 🇺🇸 United States

VEGA

DI: 04046955286010 · Model: ME784 · AESCULAP IMPLANT SYSTEMS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
VEGA
Primary DI
04046955286010
Version / Model
ME784
Catalog Number
ME784
Company Name
AESCULAP IMPLANT SYSTEMS, LLC
Labeler DUNS
622600992
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-05-16
Public Version
3
Public Version Date
2024-10-09
Public Version Status
Update
Public Device Record Key
1f8340c4-9424-4e61-8576-ebfd33a50c11
Distribution End Date
2024-10-08

Device Description

VEGA POSTERIOR REFERENCE INST TRAY BASE

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
No
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
FSM TRAY, SURGICAL, INSTRUMENT

GMDN Terms

Code Name
12143 Instrument tray, reusable

Identifiers

Type ID
Primary 04046955286010

Customer Contacts