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NuVeria Labs

FDA UDI

Class I (US FDA UDI)

by Remedium Healthcare Products

Identity

Trade Name
NuVeria Labs FDA UDI
Generic Name
Exudate-absorbent dressing, non-gel, non-antimicrobial FDA UDI
Device Name
NuVeria Labs bordered silicone foam dressing by Remedium Healthcare Products, 3x3 FDA UDI
Model / Reference
REMSF33B FDA UDI
Description
NuVeria Labs bordered silicone foam dressing by Remedium Healthcare Products, 3x3 FDA UDI

Identifiers

Primary DI / UDI-DI
00850050711032 FDA UDI
FDA Product Code
NAD FDA UDI
GMDN Term
Exudate-absorbent dressing, non-gel, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4020 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Exudate-absorbent dressing, non-gel, non-antimicrobial

NuVeria Labs by Remedium Healthcare Products — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Exudate-absorbent dressing, non-gel, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c5b8c806-0a45-4f32-b1cf-07649134392e 33 fields · synced May 29, 2026