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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Medical/surgical interventional tube/cable securement strap FDA UDI
Device Name
TUBE,SECUREMENT DEVICE,STERILE MED FDA UDI
Model / Reference
DYND7600M FDA UDI
Description
TUBE,SECUREMENT DEVICE,STERILE MED FDA UDI

Identifiers

Catalog Number
DYND7600M FDA UDI
Primary DI / UDI-DI
10884389245705 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Medical/surgical interventional tube/cable securement strap FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5240 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: Medical/surgical interventional tube/cable securement strap

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

Similar devices

Also classified as Medical/surgical interventional tube/cable securement strap.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medline Industries, Inc.

Sources (1)

  • FDA UDI d740676b-938b-4aa1-a116-6c29cd3a2a8d 35 fields · synced May 30, 2026