← Back to catalogue

Tidi

FDA UDI

Class I (US FDA UDI)

by Tidi Products, Llc

Identity

Trade Name
TIDI FDA UDI
Generic Name
Isolation gown, single-use FDA UDI
Device Name
Polyethylene, Over-the-Head, Protective Gown, ANSI/AAMI PB70:2012 Level 2 Protection FDA UDI
Model / Reference
8576A FDA UDI
Description
Polyethylene, Over-the-Head, Protective Gown, ANSI/AAMI PB70:2012 Level 2 Protection FDA UDI

Identifiers

Catalog Number
8576A FDA UDI
Primary DI / UDI-DI
00618125189342 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
Not 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

Tidi by Tidi Products, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Tidi Products, Llc

Sources (1)

  • FDA UDI cec13919-15b7-47b0-b85a-18901bdc3ac3 35 fields · synced Jun 8, 2026