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Essentia

FDA UDI

Class I (US FDA UDI)

by Precision Fabrics Group, Inc.

Identity

Trade Name
Essentia FDA UDI
Generic Name
Dry medical towel/wipe, single-use FDA UDI
Device Name
Standard Blue Low Lint Towel FDA UDI
Model / Reference
SB017026 FDA UDI
Description
Standard Blue Low Lint Towel FDA UDI

Identifiers

Primary DI / UDI-DI
00747253000103 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 17 Inch FDA UDI
Width — 26 Inch FDA UDI

Category: Dry medical towel/wipe, single-use

Essentia by Precision Fabrics Group, Inc. — 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 64c97b47-f0c5-4e01-9f5e-f4412d8d20a8 35 fields · synced May 30, 2026