DEVICE: Everlywell Blood Collection Kit (G7322011)

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Device Identifier (DI) Information
Everlywell Blood Collection Kit
3
In Commercial Distribution

Everly Health, Inc.
G7322011
HIBCC

1
125739457 *Terms of Use
No description.
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Device Characteristics
Labeling does not contain MRI Safety Information
No
No
Yes
No
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?
38092 Capillary blood collection set, home-use
A collection of devices and materials available for use by a patient/layperson outside a clinical setting to collect and, in some cases, mail a capillary blood sample to a clinical laboratory for diagnostic testing or screening purposes. The kit includes a lancet(s), a blood storage device [e.g., collection strip, dry blood collection card/filter paper card, vial] and other items (e.g., alcohol prep pad, gauze pad, bandage strip, a container with a requisition form for mailing to the laboratory); some types may alternatively be in the form of a skin-attached self-contained unit and may feature a blood drawing suction mechanism. This is a single-use device.
Active false
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FDA Product Code

[?]
Product Code Product Code Name
PQD Blood Specimen Collection Convenience Kit (Excludes Hiv)
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FDA Premarket Submission
FDA Premarket Submission Number [?] Supplement Number [?]
Premarket Submission Number Not Available/Not Released
Yes CLOSE

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

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Storage and Handling
No storage/handling found
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Clinically Relevant Size

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Size Type Text
No Device Sizes
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Device Record Status
3ff921ef-7d34-408f-9a3c-6030dfbb7d03
May 18, 2026
4
February 14, 2025
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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

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

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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

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Yes
No
Yes
No
No CLOSE

Customer Contact

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No Customer Contact currently defined
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