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Proteger

FDA UDI

Class II (US FDA UDI)

by DAS Medical International SRL

Identity

Trade Name
Proteger FDA UDI
Generic Name
Medical equipment/instrument drape, single-use FDA UDI
Device Name
Zeiss 65D Surgical Protection System 53" X 120" (ZP6553120) FDA UDI
Model / Reference
ZP6553120 FDA UDI
Description
Zeiss 65D Surgical Protection System 53" X 120" (ZP6553120) FDA UDI

Identifiers

Catalog Number
ZP6553120 FDA UDI
Primary DI / UDI-DI
07466532979147 FDA UDI
FDA Product Code
PUI FDA UDI
GMDN Term
Medical equipment/instrument drape, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Medical equipment/instrument drape, single-use

Proteger by DAS Medical International SRL — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical equipment/instrument drape, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3716765c-9aaf-4253-8982-cb297ca6de6e 35 fields · synced Jun 1, 2026