DEVICE: Contact Lens, HD Professional, Cohen-Benner, "CBC" (00852475007202)

Device Identifier (DI) Information

Contact Lens, HD Professional, Cohen-Benner, "CBC"
54013
In Commercial Distribution
54013
OCULUS SURGICAL INC
00852475007202
GS1

1
015409582 *Terms of Use
1 Each 54013 Contact Lens, HD Professional, Cohen-Benner Contact "CBC"
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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?
58070 Vitrectomy contact lens, single-use
A sterile ophthalmic lens intended to be placed on the cornea of a patient to improve visualization of the fundus and retinal structures by surgical staff using an ophthalmic microscope during vitreoretinal surgery. Also known as a vitrectomy sutureless lens (VSL), it is made of various transparent materials [e.g., polymethylmethacrylate (PMMA), glass, quartz]. This is a single-use device.
Active false
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FDA Product Code

[?]
Product Code Product Code Name
HJK Lens, Contact, Polymethylmethacrylate, Diagnostic
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FDA Premarket Submission

FDA Premarket Submission Number [?] Supplement Number [?]
K051630 000
No CLOSE

Sterilization

Yes
No
Sterilization Method [?]
No Sterilization Methods Found
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Storage and Handling

[?]
Storage and Handling
Storage Environment Temperature: between -10 and 50 Degrees Celsius
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Clinically Relevant Size

[?]
Size Type Text
Outer Diameter: 13.6 Millimeter
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Device Record Status

258d8ed9-0a8e-40db-9d03-0a0aa0e89799
June 02, 2021
3
February 26, 2021
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Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]
Package DI Number Quantity per Package Contains DI Package Package Discontinue Date Package Status Package Type
10852475007209 10 00852475007202 In Commercial Distribution Case
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Secondary DI

[?]
Issuing Agency [?] Secondary DI Number
No Secondary DIs found
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Unit of Use DI

[?]
Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]
No
No
None
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Production Identifier(s) in UDI

[?]
Yes
No
Yes
Yes
No CLOSE

Customer Contact

[?]
7722362622
info@oculussurgical.com
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