Cer-Rmr-8

FDA UDI

Class I (US FDA UDI)

by Ranfac Corp.

Identity

Trade Name: CER-RMR-8 FDA UDI
Generic Name: Bone-resection orthopaedic reamer, single-use FDA UDI
Device Name: Cervos 8GA Reamers P/N: 74370-01M Customer #: 12153 FDA UDI
Model / Reference: 8GA X 7" FDA UDI
Description: Cervos 8GA Reamers P/N: 74370-01M Customer #: 12153 FDA UDI

Identifiers

Catalog Number: CER-RMR-8 FDA UDI
Primary DI / UDI-DI: 00850023741110 FDA UDI
FDA Product Code: HTO FDA UDI
GMDN Term: Bone-resection orthopaedic reamer, single-use 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

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size: Length — 7 Inch FDA UDI
Outer Diameter — 0.131 Inch FDA UDI

Category: Bone-resection orthopaedic reamer, single-use

Cer-Rmr-8 by Ranfac Corp. — 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: Ranfac Corp.

Sources (1)

FDA UDI 7c8d56d5-31d8-4096-b2e7-d5e756052308 36 fields · synced May 29, 2026