DEVICE: OP - First aid series (06974686050014)
Device Identifier (DI) Information
OP - First aid series
OP301
In Commercial Distribution
Yiwu Ori-Power Medtech Co.,Ltd.
OP301
In Commercial Distribution
Yiwu Ori-Power Medtech Co.,Ltd.
No description.
Device Characteristics
Labeling does not contain MRI Safety Information | |
No | |
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Yes | |
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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? |
---|---|---|---|---|
12135 | Insect bite/sting kit |
A convenient collection of the necessary instruments, pharmaceuticals, and other items needed in an emergency to inject epinephrine into a victim who has sustained an insect bite or sting. This is a single-use device.
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Active | false |
10516 | Burn kit, non-medicated |
A collection of devices designed to treat first or second degree burns typically as first aid therapy by emergency medical services (EMS); it does not include pharmaceuticals. It typically includes burn dressings, burn gels, gauze, cold packs, adhesive tapes, and gloves; it may include additional devices such as scissors and masks. This is a single-use device.
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Active | false |
13913 | Antiseptic skin swab |
A device that is pre-soaked with an antiseptic and intended to inhibit the growth of microorganisms on the skin; it may also include an anaesthetic to alleviate pain. It is typically designed as a sterile cotton swab (a pledget) on a plastic stick and used in the hospital environment, in the home, or carried for first aid to prevent infection and provide temporary pain and itching relief associated with minor cuts, scrapes, or burns. This is a single-use device.
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Active | false |
FDA Product Code
[?]Product Code | Product Code Name |
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LRR | First Aid Kit With Drug |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
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Premarket Submission Number Not Available/Not Released |
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
5ef45c4d-ebdc-4b5f-b2aa-9ce10619688f
October 18, 2023
2
February 25, 2022
October 18, 2023
2
February 25, 2022
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
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No Package DIs found |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
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No Secondary DIs found |
Unit of Use DI
[?]
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