Sterilization Wrap, Reliance Solo S200

FDA UDI

Class II (US FDA UDI)

by Ahlstrom Nonwovens Llc

Identity

Trade Name: Sterilization Wrap, Reliance Solo S200 FDA UDI
Generic Name: Sterilization packaging, single-use FDA UDI
Device Name: WLJ1Z1086B, Sterilization Wrap, Reliance Solo 200, 54 x 54 inches [] 96 sheets/case, 2 bonded sheets per application = 48 applications/case. Wrap with Green layer on outside. Review IFU. FDA UDI
Model / Reference: WLJ1Z1086B54 FDA UDI
Description: WLJ1Z1086B, Sterilization Wrap, Reliance Solo 200, 54 x 54 inches [] 96 sheets/case, 2 bonded sheets per application = 48 applications/case. Wrap with Green layer on outside. Review IFU. FDA UDI

Identifiers

Primary DI / UDI-DI: 00841982101442 FDA UDI
FDA Product Code: FRG 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

Sterilization Wrap, Reliance Solo S200 by Ahlstrom Nonwovens Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: Ahlstrom Nonwovens Llc

Sources (1)

FDA UDI 7a3ef3c7-039e-40ab-a53e-113cbf88b91d 34 fields · synced May 30, 2026