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Eclipse PRP PRP1000-B

by Eclipse, Inc.

Eclipse PRP PRP1000-B is a device made by Eclipse, Inc., listed in FDA GUDID since 4 Oct 2018 (UDI-DI 00853602008031), 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 Number00853602008031 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  • Withdrawn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
Blood collection set, invasive
Model / Ref / Catalog
PRP1000-B
Primary DI / UDI-DI
00853602008031
GMDN term
Blood collection set, invasive
GUDID distribution status
In Commercial Distribution
Size
Weight — 39.4 Gram
Depth — 1.125 Inch
Width — 6.928 Inch
Height — 3.125 Inch

Related devices

Category: Blood collection set, invasive

Similar devices in this category

Other devices filed under Blood collection set, invasive.

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)