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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
Laparoscopic access cannula, reprocessed FDA UDI
Device Name
B12SRT ENDPH XCEL BLADELESS TROCAR, W/S FDA UDI
Model / Reference
B12SRTR FDA UDI
Description
B12SRT ENDPH XCEL BLADELESS TROCAR, W/S FDA UDI

Identifiers

Catalog Number
B12SRTR FDA UDI
Primary DI / UDI-DI
10888277386143 FDA UDI
FDA Product Code
NLM FDA UDI
GMDN Term
Laparoscopic access cannula, reprocessed FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Laparoscopic access cannula, reprocessed

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

Similar devices

Also classified as Laparoscopic access cannula, reprocessed.

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 cea1ef33-1387-441c-91a4-c7bd56eb422e 35 fields · synced Jun 8, 2026