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Master

FDA UDI

Class I (US FDA UDI)

by Dongguan Maisite Medical Instruments Co., Ltd.

Identity

Trade Name
Master FDA UDI
Generic Name
Postsurgical eye shield, vented FDA UDI
Model / Reference
Metal FDA UDI

Identifiers

Primary DI / UDI-DI
06975374678015 FDA UDI
FDA Product Code
HMP FDA UDI
GMDN Term
Postsurgical eye shield, vented FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4440 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Postsurgical eye shield, vented

Master by Dongguan Maisite Medical Instruments Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Postsurgical eye shield, vented.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1d9be73a-ed4c-4043-a87f-debc2b465750 32 fields · synced Jun 8, 2026