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Surgiplus

FDA UDI

Class I (US FDA UDI)

by A Plus International, Inc

Identity

Trade Name
SURGIPLUS FDA UDI
Generic Name
Isolation gown, single-use FDA UDI
Device Name
P/E FILM GOWN BLUE;1/BG, 15 BG/BX, 5 BX/CS FDA UDI
Model / Reference
1 FDA UDI
Description
P/E FILM GOWN BLUE;1/BG, 15 BG/BX, 5 BX/CS FDA UDI

Identifiers

Catalog Number
68-6201-B FDA UDI
Primary DI / UDI-DI
00683534060544 FDA UDI
FDA Product Code
LYU 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Isolation gown, single-use

Surgiplus by A Plus International, Inc — 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

Sources (1)

  • FDA UDI b323f178-1d71-445e-bdb4-a783e42150ba 34 fields · synced May 30, 2026