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Bone File #64x Cross Cut Hd D/E

FDA UDI

Class I (US FDA UDI)

by W.H. Holden, Inc.

Identity

Trade Name
BONE FILE #64X CROSS CUT HD D/E FDA UDI
Generic Name
Bone file/rasp, reciprocating, single-use FDA UDI
Model / Reference
10-5264XHD FDA UDI

Identifiers

Primary DI / UDI-DI
D928105264XHD0 FDA UDI
FDA Product Code
EMI FDA UDI
GMDN Term
Bone file/rasp, reciprocating, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone file/rasp, reciprocating, single-use

Bone File #64x Cross Cut Hd D/E by W.H. Holden, 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

Manufacturer
W.H. Holden, Inc.

Sources (1)

  • FDA UDI 01a122a6-89bb-4ef7-b14e-00c9f4ad05e8 32 fields · synced May 29, 2026