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Starling Medical, Inc

FDA UDI

Class I (US FDA UDI)

by Starling Medical

Identity

Trade Name
Starling Medical, Inc FDA UDI
Generic Name
Multiple urine analyte IVD, kit, rapid colorimetric, self-testing FDA UDI
Device Name
Anchor Assembly FDA UDI
Model / Reference
DW-01206 FDA UDI
Description
Anchor Assembly FDA UDI

Identifiers

Primary DI / UDI-DI
00860010249017 FDA UDI
FDA Product Code
JMT FDA UDI
GMDN Term
Multiple urine analyte IVD, kit, rapid colorimetric, self-testing FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1510 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multiple urine analyte IVD, kit, rapid colorimetric, self-testing

Starling Medical, Inc by Starling Medical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple urine analyte IVD, kit, rapid colorimetric, self-testing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Starling Medical

Sources (1)

  • FDA UDI a5cf048b-5e27-4b0a-9173-82a327d5904c 33 fields · synced May 31, 2026