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Eclipse PRP PRP1000.Intl

by Eclipse, Inc.

Eclipse PRP PRP1000.Intl is a Class II device made by Eclipse, Inc., listed in FDA GUDID since 4 Oct 2018 (UDI-DI 00853602008062), 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 Number00853602008062 UDI-DI Date4 Oct 2018ListedStatusListed 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  • Withdrawn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
Eclipse PRP
Generic name
Haematological concentrate system
Model / Ref / Catalog
PRP1000.Intl
Primary DI / UDI-DI
00853602008062
FDA product code
ORG
GMDN term
Haematological concentrate system
Device class
Class II
Regulation number
864.9245
GUDID distribution status
In Commercial Distribution
Size
Weight — 39.0 Gram
Depth — 1.250 Inch
Width — 6.438 Inch
Height — 7.094 Inch

Related devices

Category: Haematological concentrate system

Similar devices

Other devices filed under FDA product code ORG (Platelet And Plasma Separator For Bone Graft Handling).

Other devices from Eclipse, Inc.

See all devices from Eclipse, Inc. →

Properties

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