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Tidi

FDA UDI

Class I (US FDA UDI)

by Tidi Products, Llc

Identity

Trade Name
TIDI FDA UDI
Generic Name
Medical equipment/instrument drape, single-use FDA UDI
Device Name
TIDI Positioning Aids - Rectangles Frosty Ether Foam 6 Mil Vinyl 4in x 6in x 1in 4 per Set FDA UDI
Model / Reference
126-8 FDA UDI
Description
TIDI Positioning Aids - Rectangles Frosty Ether Foam 6 Mil Vinyl 4in x 6in x 1in 4 per Set FDA UDI

Identifiers

Catalog Number
126-8 FDA UDI
Primary DI / UDI-DI
01618125147174 FDA UDI
FDA Product Code
KKJ FDA UDI
GMDN Term
Medical equipment/instrument drape, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.1850 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

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

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Manufacturer

Manufacturer
Tidi Products, Llc

Sources (1)

  • FDA UDI 614ffc04-2433-45be-bb43-b67689812e7e 35 fields · synced May 31, 2026