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3M™ Attest™

FDA UDI

Class I (US FDA UDI)

by 3m Company

Identity

Trade Name
3M™ Attest™ FDA UDI
Generic Name
Instrument tray corner protector, single-use FDA UDI
Device Name
3M™ Attest™ Instrument Protectors, 5 1/2 in x 9 1/2 in, 100 Each/Pack, 10 Packs/Case FDA UDI
Model / Reference
13915 FDA UDI
Description
3M™ Attest™ Instrument Protectors, 5 1/2 in x 9 1/2 in, 100 Each/Pack, 10 Packs/Case FDA UDI

Identifiers

Catalog Number
13915 FDA UDI
Primary DI / UDI-DI
10707387792029 FDA UDI
FDA Product Code
LXZ FDA UDI
GMDN Term
Instrument tray corner protector, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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: Instrument tray corner protector, single-use

3M™ Attest™ by 3m Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument tray corner protector, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
3m Company

Sources (1)

  • FDA UDI f7edb9ae-8d56-42c5-8778-7ffb0fffad69 35 fields · synced May 30, 2026