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Hilo Fit

FDA UDI

Class I (US FDA UDI)

by Hilo Industries LLC

Identity

Trade Name
Hilo Fit FDA UDI
Generic Name
Isolation gown, single-use FDA UDI
Device Name
Hilo Fit Isolation Gown, Size LARGE, SINGLE USE ONLY, LEVEL 2 AAMI PB70, Meets requirement of Specification F3352. Available in colors blue or yellow. FDA UDI
Model / Reference
22003L FDA UDI
Description
Hilo Fit Isolation Gown, Size LARGE, SINGLE USE ONLY, LEVEL 2 AAMI PB70, Meets requirement of Specification F3352. Available in colors blue or yellow. FDA UDI

Identifiers

Primary DI / UDI-DI
00810107330227 FDA UDI
FDA Product Code
OEA FDA UDI
GMDN Term
Isolation gown, single-use 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

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

Yes

FDA UDI

Category: Isolation gown, single-use

Hilo Fit by Hilo Industries LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Isolation gown, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hilo Industries LLC

Sources (1)

  • FDA UDI 25a2a1fc-3266-4a30-a7a4-c98c14ba1934 33 fields · synced May 30, 2026