DEVICE: EVA NEXUS™ Combined 25G TDC Pack (08717872034768)
Device Identifier (DI) Information
EVA NEXUS™ Combined 25G TDC Pack
9310.25G02-00
In Commercial Distribution
9310.25G02-00
D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
9310.25G02-00
In Commercial Distribution
9310.25G02-00
D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
No description.
Device Characteristics
Labeling does not contain MRI Safety Information | |
No | |
No | |
Yes | |
Yes | |
No | |
No | |
No | |
No |
GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
---|---|---|---|---|
45150 | Ophthalmic surgical procedure kit, non-medicated, single-use |
A collection of various ophthalmic surgical instruments and the necessary materials intended to be used to perform an ophthalmic surgical procedure; it is not comprised exclusively of dedicated implantation tools and it does not contain any pharmaceuticals. This is a single-use device.
|
Active | false |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
HQE | Instrument, Vitreous Aspiration And Cutting, Ac-Powered |
HQC | Unit, Phacofragmentation |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
---|---|
K213467 | 000 |
Sterilization
Storage and Handling
[?]Storage and Handling |
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No storage/handling found |
Clinically Relevant Size
[?]Size Type Text |
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No Device Sizes |
Device Record Status
3cef5248-2dba-46d7-9a1c-f42583830ce1
February 28, 2024
1
February 20, 2024
February 28, 2024
1
February 20, 2024
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
---|---|---|---|---|---|
No Package DIs found |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
---|---|
No Secondary DIs found |
Unit of Use DI
[?]
Unit of Use DI Number:
18717872034765
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
No Customer Contact currently defined