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maxill Silkenhttps://gudid.fda.gov/gudid/a Earloop Style Procedural Masks, Green

FDA UDI

Class II (US FDA UDI)

by Maxill, Inc.

Identity

Trade Name
maxill Silkenhttps://gudid.fda.gov/gudid/a Earloop Style Procedural Masks, Green FDA UDI
Generic Name
Surgical/medical face mask, single-use FDA UDI
Model / Reference
53033 FDA UDI

Identifiers

Primary DI / UDI-DI
00060705530332 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
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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical/medical face mask, single-use

maxill Silkenhttps://gudid.fda.gov/gudid/a Earloop Style Procedural Masks, Green by Maxill, Inc. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Surgical/medical face mask, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Maxill, Inc.

Sources (1)

  • FDA UDI cc2e8d25-2263-4b23-b10b-ed8c3b974c9f 32 fields · synced May 29, 2026