DEVICE: HYGITECH (03615140000192)
Device Identifier (DI) Information
HYGITECH
HY-07106
In Commercial Distribution
HY-07106
HYGITECH
HY-07106
In Commercial Distribution
HY-07106
HYGITECH
The HYGITECH loupe is an optical instrument developed to facilitate visualisation of specific objects or areas. It was conceived for all precise work as well as helping improve performance of dental surgeons during technical procedures.
Characteristics :
• A Velcro strap allows comfortable adjustment of the loupe around the head
• The loupe can be moved up and down to better align the eyes with the magnified area
• The unbreakable lenses protect the eyes, help your eyes adjust quickly and comfortably and give the exact hue of the magnified object
• Available in two magnifications, x2.5 or x3.5
Ergonomic
- Perfectly adjustable around the head, the loupe’s ergonomics offer true comfort and incomparable ease of use.
Light
- Weighing only 70g, the HYGITECH loupe is remarkably light.
Practical
- Allowing assistance during technical procedures, the loupe helps give the dental surgeon a better approach to the surgical field
Device Characteristics
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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? |
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12319 | Lens loop, reusable |
A hand-held, manual, ophthalmic surgical instrument designed for eye lens extraction and gentle manipulation and/or irrigation of eye tissues during an ophthalmic surgical procedure. It typically consists of a small wire loop (frequently serrated) at the distal tip and a handle for easy manipulation; it may also include a channel (e.g., a cannula) which is connected to an external irrigator for irrigation of the eye. This is a reusable device.
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Active | false |
FDA Product Code
[?]Product Code | Product Code Name |
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FXX | Mask, Surgical |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
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K173062 | 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
db9b831a-ee8d-477a-8f34-345c703c9556
December 22, 2020
1
December 14, 2020
December 22, 2020
1
December 14, 2020
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
---|---|---|---|---|---|
03615140000208 | 12 | 03615140000192 | In Commercial Distribution | Box |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
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No Secondary DIs found |
Unit of Use DI
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Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
No Customer Contact currently defined