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Convertors

FDA UDI

Class II (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
CONVERTORS FDA UDI
Generic Name
Surgical towel FDA UDI
Device Name
Absorbent Towel Bulk Non sterile FDA UDI
Model / Reference
5550- FDA UDI
Description
Absorbent Towel Bulk Non sterile FDA UDI

Identifiers

Catalog Number
5550- FDA UDI
Primary DI / UDI-DI
50630140930438 FDA UDI
FDA Product Code
PUI FDA UDI
GMDN Term
Surgical towel FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 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

Yes

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
Ethylene Oxide FDA UDI

Category: Surgical towel

Convertors by Cardinal Health 200, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical towel.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 306c66bd-a561-460d-9dc2-027c30fe55b0 34 fields · synced Jun 8, 2026