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Alleset

FDA UDI

Class II (US FDA UDI)

by GRI Medical & Electronic Technology Co., Ltd.

Identity

Trade Name
Alleset FDA UDI
Generic Name
Stockinette FDA UDI
Device Name
Impervious stockinette_Shoulder Suspension with hook_9'' x 37”_non-sterile_50EA/CS FDA UDI
Model / Reference
Model 85-SS0937 FDA UDI
Description
Impervious stockinette_Shoulder Suspension with hook_9'' x 37”_non-sterile_50EA/CS FDA UDI

Identifiers

Primary DI / UDI-DI
16931918138152 FDA UDI
FDA Product Code
PUI FDA UDI
GMDN Term
Stockinette FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 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: Stockinette

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

Similar devices

Also classified as Stockinette.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 71555068-e185-4609-a538-49d80e9f0a4d 34 fields · synced Sep 18, 2026