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Cervos Filter Assembly CER-FIL

by Ranfac Corp.

Cervos Filter Assembly CER-FIL is a Class I device made by Ranfac Corp., listed in FDA GUDID since 27 Sep 2021 (UDI-DI 00850023741394), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850023741394 UDI-DI Date27 Sep 2021ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Cervos Filter Assembly
Generic name
Bone graft harvesting filter
Model / Ref / Catalog
CER-FIL
Primary DI / UDI-DI
00850023741394
FDA product code
KET
GMDN term
Bone graft harvesting filter
Device class
Class I
Regulation number
864.3010
GUDID distribution status
In Commercial Distribution
Size
Pore Size — 150 Micrometer

Similar devices

Other devices filed under FDA product code KET (Filters, Cell Collection, Tissue Processing).

Other devices from Ranfac Corp.

See all devices from Ranfac Corp. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)