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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
Woven gauze roll/sheet FDA UDI
Model / Reference
Polyester Fiber FDA UDI

Identifiers

Primary DI / UDI-DI
06975374671016 FDA UDI
FDA Product Code
ITG FDA UDI
GMDN Term
Woven gauze roll/sheet FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3025 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Woven gauze roll/sheet

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 Woven gauze roll/sheet.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b27efc63-51e7-4e4a-ab07-824bcbc08150 32 fields · synced Jun 8, 2026