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CeroFrict

FDA UDI

Class I (US FDA UDI)

by SML Med-Tech Solutions Limited

Identity

Trade Name
CeroFrict FDA UDI
Generic Name
Instrument tray cover, single-use FDA UDI
Device Name
Disposable Protective Liner FDA UDI
Model / Reference
SML011-PL01-BBP FDA UDI
Description
Disposable Protective Liner FDA UDI

Identifiers

Primary DI / UDI-DI
04897129991342 FDA UDI
FDA Product Code
PHT FDA UDI
GMDN Term
Instrument tray cover, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.1500 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Instrument tray cover, single-use

CeroFrict by SML Med-Tech Solutions Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument tray cover, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2943ff5b-096f-46d6-bcd5-0e638eb4f087 33 fields · synced May 30, 2026