← Back to catalogue

Medline Industries, Inc.

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE INDUSTRIES, INC. FDA UDI
Generic Name
Chemical/physical sterilization process indicator FDA UDI
Device Name
DBD-PACK,BIOLOGICAL TEST,FOR GAS FDA UDI
Model / Reference
MDS200550 FDA UDI
Description
DBD-PACK,BIOLOGICAL TEST,FOR GAS FDA UDI

Identifiers

Catalog Number
MDS200550 FDA UDI
Primary DI / UDI-DI
10080196314942 FDA UDI
FDA Product Code
FRG FDA UDI
GMDN Term
Chemical/physical sterilization process indicator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6850 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Chemical/physical sterilization process indicator

Medline Industries, Inc. by Medline Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Chemical/physical sterilization process indicator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Medline Industries, Inc.

Sources (1)

  • FDA UDI 83249c5f-b6c6-47a9-878a-2120ffd285ff 35 fields · synced May 30, 2026