HEPRO.US Lab Suit - Case

FDA UDI

Class I (US FDA UDI)

by Hepro.us Inc.

Identity

Trade Name: HEPRO.US Lab Suit - Case FDA UDI
Generic Name: Surgical/examination garment kit FDA UDI
Device Name: Material 43gsm A/S SMMS Color: Green - In Bulk, 50pcs/Ctn FDA UDI
Model / Reference: CT Lab Suit FDA UDI
Description: Material 43gsm A/S SMMS Color: Green - In Bulk, 50pcs/Ctn FDA UDI

Identifiers

Primary DI / UDI-DI: 00854427007087 FDA UDI
FDA Product Code: FXO FDA UDI
GMDN Term: Surgical/examination garment kit FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4040 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Safe FDA UDI

Category: Surgical/examination garment kit

HEPRO.US Lab Suit - Case by Hepro.us Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Hepro.us Inc.

Sources (1)

FDA UDI a8c38b31-290b-4403-9244-ca4c9009a0af 33 fields · synced May 30, 2026