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Medline Renewal

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE RENEWAL FDA UDI
Generic Name
Surgical saw blade, sagittal, reprocessed FDA UDI
Device Name
5071-323 HALL INTREX BLADE SYS 1.19MM FDA UDI
Model / Reference
5071323R FDA UDI
Description
5071-323 HALL INTREX BLADE SYS 1.19MM FDA UDI

Identifiers

Catalog Number
5071323R FDA UDI
Primary DI / UDI-DI
10888277368446 FDA UDI
FDA Product Code
GFA FDA UDI
GMDN Term
Surgical saw blade, sagittal, reprocessed FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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: Surgical saw blade, reciprocating, reprocessedSurgical saw blade, sagittal, reprocessed

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

Similar devices

Also classified as Surgical saw blade, sagittal, reprocessed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f7597994-543f-4dc6-9263-d049ad1c36ca 35 fields · synced May 30, 2026