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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
Emphysematous lung sealant FDA UDI
Model / Reference
gel FDA UDI

Identifiers

Primary DI / UDI-DI
06975374671214 FDA UDI
FDA Product Code
NAD FDA UDI
GMDN Term
Emphysematous lung sealant FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4020 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

Yes

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: Emphysematous lung sealant

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6744447d-12a5-4568-82e8-5c71e9257fe8 32 fields · synced Jun 7, 2026