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Espe™

FDA UDI

Class II (US FDA UDI)

by 3m Company

Identity

Trade Name
ESPE™ FDA UDI
Generic Name
Surgical/medical face mask, single-use FDA UDI
Device Name
3M™ ESPE™ Molded Face Masks, Blue, 1942FB FDA UDI
Model / Reference
1942FB FDA UDI
Description
3M™ ESPE™ Molded Face Masks, Blue, 1942FB FDA UDI

Identifiers

Catalog Number
1942FB FDA UDI
Primary DI / UDI-DI
30605861032316 FDA UDI
FDA Product Code
FXX FDA UDI
GMDN Term
Surgical/medical face mask, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4040 FDA UDI
Commercial Distribution
Not 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

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
3m Company

Sources (1)

  • FDA UDI 82de17eb-0c53-478a-886a-d528dd6295bb 36 fields · synced Jun 1, 2026