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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
Synthetic polymer semi-permeable film dressing, adhesive FDA UDI
Device Name
Transparent Film Dressing, 6x7cm, Waterproof, Sterile FDA UDI
Model / Reference
RMTD1 FDA UDI
Description
Transparent Film Dressing, 6x7cm, Waterproof, Sterile FDA UDI

Identifiers

Primary DI / UDI-DI
00850037100507 FDA UDI
FDA Product Code
KMK FDA UDI
GMDN Term
Synthetic polymer semi-permeable film dressing, adhesive FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5210 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: Synthetic polymer semi-permeable film dressing, adhesive

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 Synthetic polymer semi-permeable film dressing, adhesive.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 74a791f8-26d4-45f5-b000-5b1c99312c4d 33 fields · synced Jun 8, 2026