← Back to catalogue

Alleset

FDA UDI

Class I (US FDA UDI)

by GRI Medical & Electronic Technology Co., Ltd.

Identity

Trade Name
Alleset FDA UDI
Generic Name
Operating room turnover kit FDA UDI
Device Name
Mattress cover_Heel slope_80in_12PCS FDA UDI
Model / Reference
HSM3680 FDA UDI
Description
Mattress cover_Heel slope_80in_12PCS FDA UDI

Identifiers

Primary DI / UDI-DI
16931918152752 FDA UDI
FDA Product Code
FMW FDA UDI
GMDN Term
Operating room turnover kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6190 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Operating room turnover kit

Alleset by GRI Medical & Electronic Technology Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Operating room turnover kit.

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 61382f7a-d231-4a3f-9482-c4abc5d54880 34 fields · synced Sep 18, 2026