← Back to catalogue

Master

FDA UDI

Class I (US FDA UDI)

by Dongguan Maisite Medical Instruments Co., Ltd.

Identity

Trade Name
Master FDA UDI
Generic Name
Rescue blanket, reusable FDA UDI
Model / Reference
PET FDA UDI

Identifiers

Primary DI / UDI-DI
06975374671511 FDA UDI
FDA Product Code
KME FDA UDI
GMDN Term
Rescue blanket, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6060 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: Rescue blanket, reusable

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 Rescue blanket, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI c1ac35ce-11aa-4fb4-b8d3-50c4f81dc2c9 32 fields · synced May 30, 2026