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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
Tourniquet cuff, single-use FDA UDI
Device Name
Pneumatic Surgical Tourniquet - Sterile, Single-Use, Single Bladder, Dual Port, Size: M, 24", Color: Pink FDA UDI
Model / Reference
RMST24SU FDA UDI
Description
Pneumatic Surgical Tourniquet - Sterile, Single-Use, Single Bladder, Dual Port, Size: M, 24", Color: Pink FDA UDI

Identifiers

Primary DI / UDI-DI
00850037100446 FDA UDI
FDA Product Code
QGX FDA UDI
GMDN Term
Tourniquet cuff, single-use 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

Yes

FDA UDI

Single Use

Yes

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: Tourniquet cuff, single-use

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 Tourniquet cuff, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6ffd0b40-9ec8-4c65-b952-87e96126782b 33 fields · synced May 29, 2026