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GelShot

FDA UDI

Class II (US FDA UDI)

by Compass Health Brands Corp.

Identity

Trade Name
GelShot FDA UDI
Generic Name
Ultrasound coupling pad holder FDA UDI
Device Name
RICHMAR WINNER EVO 2CM US ADAPTOR, CASE OF 10 FDA UDI
Model / Reference
GSA2RM1 FDA UDI
Description
RICHMAR WINNER EVO 2CM US ADAPTOR, CASE OF 10 FDA UDI

Identifiers

Primary DI / UDI-DI
10850958007111 FDA UDI
FDA Product Code
MUI FDA UDI
GMDN Term
Ultrasound coupling pad holder FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1570 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

GelShot by Compass Health Brands Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7bca44af-3314-4f76-ad02-e06875bb86b2 35 fields · synced Jun 1, 2026