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maxill Safeguard Paper Sterilization Wrap - 12" x 12" Crepe Paper

FDA UDI

Class II (US FDA UDI)

by Maxill, Inc.

Identity

Trade Name
maxill Safeguard Paper Sterilization Wrap - 12" x 12" Crepe Paper FDA UDI
Generic Name
Instrument/equipment drape, single-use, non-sterile FDA UDI
Model / Reference
60160 FDA UDI

Identifiers

Primary DI / UDI-DI
00060705601605 FDA UDI
FDA Product Code
FRG FDA UDI
GMDN Term
Instrument/equipment drape, single-use, non-sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6850 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

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Instrument/equipment drape, single-use, non-sterile

maxill Safeguard Paper Sterilization Wrap - 12" x 12" Crepe Paper by Maxill, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument/equipment drape, single-use, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Maxill, Inc.

Sources (1)

  • FDA UDI a9444364-12aa-4062-8645-5156a3eceaa9 32 fields · synced May 31, 2026