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Ranfac Filter Assembly

FDA UDI

Class I (US FDA UDI)

by Ranfac Corp.

Identity

Trade Name
Ranfac Filter Assembly FDA UDI
Generic Name
Bone graft harvesting filter FDA UDI
Device Name
Ranfac Filter Assembly, F/G, Sterile PN 76080-01M FDA UDI
Model / Reference
RAN-FILTER FDA UDI
Description
Ranfac Filter Assembly, F/G, Sterile PN 76080-01M FDA UDI

Identifiers

Catalog Number
RAN-FILTER FDA UDI
Primary DI / UDI-DI
00858690006303 FDA UDI
FDA Product Code
KET FDA UDI
GMDN Term
Bone graft harvesting filter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3010 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Pore Size — 150 Micrometer FDA UDI

Category: Bone graft harvesting filter

Ranfac Filter Assembly by Ranfac Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone graft harvesting filter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ranfac Corp.

Sources (1)

  • FDA UDI d925346b-8108-4963-9cc5-56390fb82d5f 36 fields · synced Jun 1, 2026