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Aegis Personal Protective Suit

FDA UDI

Class I (US FDA UDI)

by Cao Group, Inc.

Identity

Trade Name
Aegis Personal Protective Suit FDA UDI
Generic Name
Professional examination gown, reusable FDA UDI
Device Name
Single use 2-piece protective suit. Small size. FDA UDI
Model / Reference
005-00059 FDA UDI
Description
Single use 2-piece protective suit. Small size. FDA UDI

Identifiers

Primary DI / UDI-DI
00872320005221 FDA UDI
FDA Product Code
OEA FDA UDI
GMDN Term
Professional examination gown, reusable 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

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

Yes

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: Professional examination gown, reusable

Aegis Personal Protective Suit by Cao Group, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Professional examination gown, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cao Group, Inc.

Sources (1)

  • FDA UDI 1abeb070-5650-4d9b-9a18-3785d4dc0798 33 fields · synced May 30, 2026