Mtehfyaf My-Fzs-01

by Beijing Xingjian Yongzhen Technology Co., Ltd.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number06975029700061 UDI-DI	Date12 Jun 2024Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Mtehfyaf
Generic Name: Rebreathing oxygen face mask
Model / Reference: MY-FZS-01

Primary DI / UDI-DI: 06975029700061
FDA Product Code: BYW
GMDN Term: Rebreathing oxygen face mask

Device Class: Class I
Regulation Number: 868.5675
GUDID distribution status: In Commercial Distribution

Other devices from Beijing Xingjian Yongzhen Technology Co., Ltd.

Mtehfyaf My-Fyy-03

Class I
Mtehfyaf My-Qyj-01

Class I

Properties

Premarket Exempt
Lot / Batch Number
Expiration Date

Other properties (11)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Prescription Use: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Serial Number: No
Manufacturing Date: No