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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
Laboratory apron FDA UDI
Device Name
COAT LAB SAFECARE LAPEL WHT XL SAFECARE LC (LAPEL COLLAR) 99% POLY 1% CARBON FDA UDI
Model / Reference
46942-WT9 FDA UDI
Description
COAT LAB SAFECARE LAPEL WHT XL SAFECARE LC (LAPEL COLLAR) 99% POLY 1% CARBON FDA UDI

Identifiers

Primary DI / UDI-DI
00609953137865 FDA UDI
FDA Product Code
LYU FDA UDI
GMDN Term
Laboratory apron FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4040 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

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Laboratory apron

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

Similar devices

Also classified as Laboratory apron.

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 80c9012f-32c6-459f-b7fa-6fb5cce21973 34 fields · synced Jun 1, 2026