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Sterile Cover Pu /10 Ea.

FDA UDI

Class II (US FDA UDI)

by Aktormed GmbH

Identity

Trade Name
STERILE COVER PU /10 EA. FDA UDI
Generic Name
Medical equipment/instrument drape, single-use FDA UDI
Device Name
10x AKTORMED PROBE COVER 30cm X 178cm (00748426105830) FDA UDI
Model / Reference
110096 FDA UDI
Description
10x AKTORMED PROBE COVER 30cm X 178cm (00748426105830) FDA UDI

Identifiers

Primary DI / UDI-DI
04260463840964 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

No

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

No

FDA UDI

Category: Medical equipment/instrument drape, single-use

Sterile Cover Pu /10 Ea. by Aktormed GmbH — 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

Manufacturer
Aktormed GmbH

Sources (1)

  • FDA UDI 7b69d0c4-7587-40c8-8157-dc270925c79c 33 fields · synced Jun 8, 2026