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Proteger ZP6553120

by DAS Medical International SRL

Proteger ZP6553120 is a Class II device made by DAS Medical International SRL, listed in FDA GUDID since 3 May 2021 (UDI-DI 07466532979147), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07466532979147 UDI-DI Date3 May 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  • Withdrawn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
Proteger
Generic name
Medical equipment/instrument drape, single-use
Model / Ref / Catalog
ZP6553120
Description
Zeiss 65D Surgical Protection System 53" X 120" (ZP6553120)
Primary DI / UDI-DI
07466532979147
FDA product code
PUI
GMDN term
Medical equipment/instrument drape, single-use
Device class
Class II
Regulation number
878.4370
GUDID distribution status
In Commercial Distribution
Sterilisation method
Ethylene Oxide

Related devices

Category: Medical equipment/instrument drape, single-use

Similar devices in this category

Other devices filed under Medical equipment/instrument drape, single-use.

Other devices from Das Medical International, SRL

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Properties

  • Supplied sterile
  • Sterilise before use
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (7, all answered No)