DEVICE: DUOVISC (00380651831353)

Device Identifier (DI) Information

DUOVISC
8065183135
In Commercial Distribution

Alcon Laboratories, Inc.
00380651831353
GS1

1
008018525 *Terms of Use
DUOVISC (0.40PRO/0.35VIS)
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Device Characteristics

Labeling does not contain MRI Safety Information
No
Yes
Yes
Yes
No
No
No
No

GMDN

[?]

GMDN Names and Definitions: © Copyright GMDN Agency 2015. Reproduced with Permission from the GMDN Agency.

GMDN Preferred Term Name GMDN Definition
Aqueous/vitreous humour replacement medium kit A collection of sterile devices, including a fluid or semifluid substance, used in combination to replace the fluid of the eye. This is a single-use device.
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FDA Product Code

[?]
Product Code Product Code Name
LZP Aid, Surgical, Viscoelastic
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FDA Premarket Submission

FDA Premarket Submission Number [?] Supplement Number [?]
Premarket Submission Number Not Available/Not Released
No CLOSE

Sterilization

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

[?]
Storage and Handling
No storage/handling found
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Clinically Relevant Size

[?]
Size Type Text
Device Size Text, specify: 0.40 mL PROVISC® OVD
Device Size Text, specify: 0.35 mL VISCOAT® OVD
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Device Record Status

51b767dc-46b6-4b46-a0ca-b28731b69882
March 29, 2018
2
March 31, 2015
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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
No Package DIs found
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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
No
No CLOSE

Customer Contact

[?]
+1(800)-862-5266
web.masterus@alcon.com
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