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Encompass

FDA UDI

Class II (US FDA UDI)

by Encompass Group, L.L.C.

Identity

Trade Name
Encompass FDA UDI
Generic Name
Sterilization packaging, reusable FDA UDI
Device Name
2 PLY WRAPPER 18X18 HEM JADE FDA UDI
Model / Reference
26184-018 FDA UDI
Description
2 PLY WRAPPER 18X18 HEM JADE FDA UDI

Identifiers

Primary DI / UDI-DI
00609953963099 FDA UDI
FDA Product Code
FRG FDA UDI
GMDN Term
Sterilization packaging, reusable 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

No

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Sterilization packaging, reusable

Encompass by Encompass Group, L.L.C. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sterilization packaging, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Encompass Group, L.L.C.

Sources (1)

  • FDA UDI 9d49228a-8190-4c2d-8c3e-457a770dd62f 34 fields · synced Jun 8, 2026