← Back to catalogue

Hawksight Drape

FDA UDI

Class I (US FDA UDI)

by Pharma Sept Medical Products (1995) Ltd.

Identity

Trade Name
HAWKSIGHT DRAPE FDA UDI
Generic Name
Medical equipment/instrument drape, single-use FDA UDI
Device Name
Operating room microscope cover FDA UDI
Model / Reference
80-562H FDA UDI
Description
Operating room microscope cover FDA UDI

Identifiers

Primary DI / UDI-DI
07290115960211 FDA UDI
FDA Product Code
HRM FDA UDI
GMDN Term
Medical equipment/instrument drape, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4700 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

Category: Medical equipment/instrument drape, single-use

Hawksight Drape by Pharma Sept Medical Products (1995) Ltd. — Class I — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI e77b6482-7163-4404-974a-83d0eec60669 33 fields · synced May 30, 2026