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AtlanticMED

FDA UDI

Class II (US FDA UDI)

by Atlantic Trading LLC

Identity

Trade Name
AtlanticMED FDA UDI
Generic Name
Surgical/medical respirator, non-antimicrobial, single-use FDA UDI
Device Name
Surgical N95 Respirator, NIOSH Approved, Berry-Compliant, Made-in-the-USA FDA UDI
Model / Reference
ATL-SUR200 FDA UDI
Description
Surgical N95 Respirator, NIOSH Approved, Berry-Compliant, Made-in-the-USA FDA UDI

Identifiers

Primary DI / UDI-DI
10860008614671 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

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

AtlanticMED by Atlantic Trading LLC — 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

Sources (1)

  • FDA UDI ed532066-8cd2-4d3a-be95-4cb5c59d5b7b 33 fields · synced Jun 8, 2026