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ACETABULAR REAMER EVO 2 Ti CUP D72 mm

FDA UDI

Class I (US FDA UDI)

by Hpf Srl

Identity

Trade Name
ACETABULAR REAMER EVO 2 Ti CUP D72 mm FDA UDI
Generic Name
Bone-resection orthopaedic reamer, single-use FDA UDI
Model / Reference
H0038557299 FDA UDI

Identifiers

Primary DI / UDI-DI
08057968717879 FDA UDI
FDA Product Code
HWE FDA UDI
GMDN Term
Bone-resection orthopaedic reamer, single-use 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

No

FDA UDI

Single Use

Yes

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-resection orthopaedic reamer, single-use

ACETABULAR REAMER EVO 2 Ti CUP D72 mm by Hpf Srl — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone-resection orthopaedic reamer, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hpf Srl

Sources (1)

  • FDA UDI 2a230099-0c44-4d68-8ea2-8f2c39fc3f0f 32 fields · synced May 30, 2026