← Back to catalogue

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
Limb tourniquet, manual, single-use FDA UDI
Device Name
TPE Tourniquet 1X18IN, Smooth Textured, Flat Pack, Orange 250/box, 4 bxs/cs FDA UDI
Model / Reference
RMDT18FPO FDA UDI
Description
TPE Tourniquet 1X18IN, Smooth Textured, Flat Pack, Orange 250/box, 4 bxs/cs FDA UDI

Identifiers

Primary DI / UDI-DI
00850037100750 FDA UDI
FDA Product Code
GAX FDA UDI
GMDN Term
Limb tourniquet, manual, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.5900 FDA UDI
Commercial Distribution
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

Yes

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: Limb tourniquet, manual, 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 Limb tourniquet, manual, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 1b497573-4f27-475e-b67a-d59e95b31dab 33 fields · synced May 30, 2026