Maytex Nupack

FDA UDI

Class II (US FDA UDI)

by Maytex Corp.

Identity

Trade Name: Maytex Nupack FDA UDI
Generic Name: Sterilization packaging, single-use FDA UDI
Device Name: See thru sterilization pouch 5 1/4" x 11" FDA UDI
Model / Reference: STP5211 FDA UDI
Description: See thru sterilization pouch 5 1/4" x 11" FDA UDI

Identifiers

Primary DI / UDI-DI: D806STP52111 FDA UDI
510(k) Number: K162258 FDA UDI
FDA Product Code: KCT FDA UDI
GMDN Term: Sterilization packaging, single-use 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Sterilization packaging, single-use

Maytex Nupack by Maytex Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Fisherbrand — FISHER SCIENTIFIC COMPANY L.L.C. · Class II

Cleared under the same submission

K162258 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Maytex Corp.

Sources (1)

FDA UDI 4a3753a9-5c2c-46f0-a89d-10e66113f63f 34 fields · synced May 30, 2026