Stripper

FDA UDI

Class I (US FDA UDI)

by KLS-Martin L.P.

Identity

Trade Name: STRIPPER FDA UDI
Generic Name: Bone file/rasp, manual, reusable FDA UDI
Device Name: PEDIATRIC, RAMUS, STEINBERG, V NOTCH, 6 MM TIP FDA UDI
Model / Reference: 48-533-02-07 FDA UDI
Description: PEDIATRIC, RAMUS, STEINBERG, V NOTCH, 6 MM TIP FDA UDI

Identifiers

Primary DI / UDI-DI: 00888118072627 FDA UDI
FDA Product Code: HRT FDA UDI
GMDN Term: Bone file/rasp, manual, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.4540 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Bone file/rasp, manual, reusable

Stripper by KLS-Martin L.P. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: KLS-Martin L.P.

Sources (1)

FDA UDI 34c62a1b-2208-4f2a-9245-29a013ec5131 35 fields · synced May 30, 2026