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Eclipse PRP HC PRP2700-LLA

by Eclipse, Inc.

Eclipse PRP HC PRP2700-LLA is a device made by Eclipse, Inc., listed in FDA GUDID since 4 Oct 2018 (UDI-DI 00853602008307), not in commercial distribution (GUDID) as of 22 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 Number00853602008307 UDI-DI Date4 Oct 2018ListedStatusListed GUDID: not 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  • Withdrawn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 HC
Generic name
Blood collection set, invasive
Model / Ref / Catalog
PRP2700-LLA
Primary DI / UDI-DI
00853602008307
GMDN term
Blood collection set, invasive
GUDID distribution status
Not in Commercial Distribution
Size
Weight — 17.000 Gram
Depth — 1.250 Inch
Width — 3.000 Inch
Height — 6.750 Inch

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)