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Resilient Medical Solutions

FDA UDI

Class I (US FDA UDI)

by Resilient Medical Solutions, LLC

Identity

Trade Name
Resilient Medical Solutions FDA UDI
Generic Name
Surgical pneumatic tourniquet system FDA UDI
Device Name
Dual to Single Port, Y Shaped Adapter, 5" FDA UDI
Model / Reference
RMSTYADAP FDA UDI
Description
Dual to Single Port, Y Shaped Adapter, 5" FDA UDI

Identifiers

Primary DI / UDI-DI
00850037100729 FDA UDI
FDA Product Code
QGX FDA UDI
GMDN Term
Surgical pneumatic tourniquet system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.5910 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

Yes

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: Surgical pneumatic tourniquet system

Resilient Medical Solutions by Resilient Medical Solutions, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical pneumatic tourniquet system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9a72da52-b0a8-41ff-a0e8-ed73ba42ca66 33 fields · synced May 30, 2026