← Back to catalogue

Steris

FDA UDI

Class II (US FDA UDI)

by Tidi Products, Llc

Identity

Trade Name
Steris FDA UDI
Generic Name
Medical equipment/instrument drape, single-use FDA UDI
Device Name
STERIS Surgical Sliding Table Drape for Velcro-less Tabletops (Disposable) FDA UDI
Model / Reference
31768 FDA UDI
Description
STERIS Surgical Sliding Table Drape for Velcro-less Tabletops (Disposable) FDA UDI

Identifiers

Catalog Number
BF549 FDA UDI
Primary DI / UDI-DI
00618125190652 FDA UDI
FDA Product Code
PUI FDA UDI
GMDN Term
Medical equipment/instrument drape, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 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: Medical equipment/instrument drape, single-use

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

Similar devices

Also classified as Medical equipment/instrument drape, single-use.

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 d25d244e-56a7-4dd8-ae56-4f577ccd07ce 34 fields · synced Jun 1, 2026