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Medline Renewal

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE RENEWAL FDA UDI
Generic Name
Endoscopic manual linear cutting stapler, reprocessed FDA UDI
Device Name
030811 @MULTIFIRE ENDO GIA W/O STAPL FDA UDI
Model / Reference
0308111R FDA UDI
Description
030811 @MULTIFIRE ENDO GIA W/O STAPL FDA UDI

Identifiers

Catalog Number
0308111R FDA UDI
Primary DI / UDI-DI
10888277368293 FDA UDI
FDA Product Code
GAG FDA UDI
GMDN Term
Endoscopic manual linear cutting stapler, reprocessed FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4740 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

Yes

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

No

FDA UDI

Category: Endoscopic manual linear cutting stapler, reprocessed

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

Similar devices

Also classified as Endoscopic manual linear cutting stapler, reprocessed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 646db8cb-4ea9-45dc-9ff8-b040227c8ddb 35 fields · synced May 30, 2026