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Weida, Jinliang

FDA UDIEUDAMED

Class II (US FDA UDI)

by Ammex-Weida (Hubei) Health and Safety Products Co., Ltd

Identity

Trade Name
WEIDA, JINLIANG FDA UDI
Generic Name
Surgical/medical face mask, antimicrobial, single-use FDA UDI
Model / Reference
A-31B FDA UDI

Identifiers

Primary DI / UDI-DI
06973219621011 FDA UDI
510(k) Number
K211062 FDA UDI
FDA Product Code
FXX FDA UDI
GMDN Term
Surgical/medical face mask, 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

No

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

Yes

FDA UDI

Category: Surgical/medical face mask, antimicrobial, single-use

Weida, Jinliang by Ammex-Weida (Hubei) Health and Safety Products Co., Ltd — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED

Similar devices

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

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ammex-Weida (Hubei) Health and Safety Products Co., Ltd

Sources (2)

  • FDA UDI 1811929c-1830-4cd3-b2dd-737e35366483 33 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 4, 2026