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Encompass

FDA UDI

Class I (US FDA UDI)

by Encompass Group, L.L.C.

Identity

Trade Name
Encompass FDA UDI
Generic Name
Dry medical towel/wipe, single-use FDA UDI
Device Name
WASHCLOTH, 12X12, 500EA TS WASHCLOTH, BLUE DIAMOND, DRC, 50/BG, 10 BG/CS NONWOVEN FDA UDI
Model / Reference
48005 FDA UDI
Description
WASHCLOTH, 12X12, 500EA TS WASHCLOTH, BLUE DIAMOND, DRC, 50/BG, 10 BG/CS NONWOVEN FDA UDI

Identifiers

Primary DI / UDI-DI
10612899001982 FDA UDI
FDA Product Code
FRL FDA UDI
GMDN Term
Dry medical towel/wipe, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5300 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

Yes

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: Dry medical towel/wipe, single-use

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

Similar devices

Also classified as Dry medical towel/wipe, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 53dbc35b-cdee-40f2-a814-9db01e8c5bba 34 fields · synced Jun 1, 2026