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Aura™

FDA UDI

Class II (US FDA UDI)

by 3m Company

Identity

Trade Name
Aura™ FDA UDI
Generic Name
Surgical/medical respirator, non-antimicrobial, single-use FDA UDI
Device Name
1870+ HEALTH CARE PART RESP. 120/CASE FDA UDI
Model / Reference
1870+ FDA UDI
Description
1870+ HEALTH CARE PART RESP. 120/CASE FDA UDI

Identifiers

Catalog Number
1870+ FDA UDI
Primary DI / UDI-DI
00051131499966 FDA UDI
FDA Product Code
MSH FDA UDI
GMDN Term
Surgical/medical respirator, non-antimicrobial, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4040 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical/medical respirator, non-antimicrobial, single-use

Aura™ by 3m Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical/medical respirator, non-antimicrobial, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
3m Company

Sources (1)

  • FDA UDI 2ee7519c-a856-482a-ac36-ef19419430ab 35 fields · synced May 30, 2026