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CellSHILED

FDA UDI

Class I (US FDA UDI)

by Equashield Medical Ltd.

Identity

Trade Name
CellSHILED FDA UDI
Generic Name
Compounding transfer set FDA UDI
Device Name
CellSHIELD Tubing Set FDA UDI
Model / Reference
LL-Set-CL FDA UDI
Description
CellSHIELD Tubing Set FDA UDI

Identifiers

Primary DI / UDI-DI
07290020288165 FDA UDI
FDA Product Code
LXG FDA UDI
GMDN Term
Compounding transfer set FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Compounding transfer set

CellSHILED by Equashield Medical Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Compounding transfer set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 34cdb247-6245-4921-ad57-a42d39c67402 33 fields · synced May 31, 2026