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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE FDA UDI
Generic Name
Bone file/rasp, reciprocating, single-use FDA UDI
Device Name
1675-125 LG COTTLE RASP 17.0MM CUT EDGE FDA UDI
Model / Reference
1675125RH FDA UDI
Description
1675-125 LG COTTLE RASP 17.0MM CUT EDGE FDA UDI

Identifiers

Catalog Number
1675125RH FDA UDI
Primary DI / UDI-DI
10888277403710 FDA UDI
FDA Product Code
HTR FDA UDI
GMDN Term
Bone file/rasp, reciprocating, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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: Bone file/rasp, reciprocating, single-use

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

Similar devices

Also classified as Bone file/rasp, reciprocating, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 44b39e9f-7f41-4204-b874-a1b3c9a01f79 35 fields · synced May 30, 2026