Skip to content

Ceros RM-PF1205

by Rhino Medical Supply Inc

Ceros RM-PF1205 is a Class II device made by Rhino Medical Supply Inc, cleared under FDA 510(k) K150143 on 31 Aug 2015 and listed in FDA GUDID since 18 Nov 2025 (UDI-DI 00810192690084), active as of 22 Oct 2026. One FDA recall is linked to it.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None ongoing

1 closed

Documents

510(k) K150143

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810192690084 UDI-DI Date18 Nov 2025ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK150143 Date31 Aug 2015DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K150143 decided 31 Aug 2015 Active
  • FDA GUDID UDI-DI 00810192690084 listed 18 Nov 2025 Listed

Recalls

1 recall · FDA

    • Terminated Z-0926-2017 FDA Class I initiated 4 Oct 2016

    Potential contamination with B. cepacia.

Timeline

3 dated events

  1. Cleared FDA 510(k) K150143
  2. Recall initiated FDA recalls Z-0926-2017
  3. Listed FDA GUDID 00810192690084

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Ceros
Generic name
Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial
Model / Ref / Catalog
RM-PF1205
Primary DI / UDI-DI
00810192690084
510(k) Number
FDA product code
NGT
GMDN term
Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial
Device class
Class II
Regulation number
880.5200
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 5 Milliliter

Related devices

Cleared under the same submission (K150143)

and 8 more cleared under K150143

Similar devices

Other devices filed under FDA product code NGT (Saline, Vascular Access Flush).

Other devices from Rhino Medical Supply Inc

  • Ceros RM-PF1210

    Class II

  • Ceros RM-PF1203

    Class II

  • Ceros RM-PF1210SF Open recall

    Class II

  • Ceros RM-CST1410

    Class I

See all devices from Rhino Medical Supply Inc →

Properties

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