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Parametrium Clamp

FDA UDI

Class I (US FDA UDI)

by adeor Medical AG

Identity

Trade Name
Parametrium Clamp FDA UDI
Generic Name
Clamp manipulation forceps FDA UDI
Model / Reference
straight 240 mm FDA UDI

Identifiers

Catalog Number
16075GY FDA UDI
Primary DI / UDI-DI
04251388900215 FDA UDI
FDA Product Code
KOH FDA UDI
GMDN Term
Clamp manipulation forceps FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.4520 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Clamp manipulation forceps

Parametrium Clamp by adeor Medical AG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Clamp manipulation forceps.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
adeor Medical AG

Sources (1)

  • FDA UDI e6f8540a-5eb1-4f21-ba4e-e4e6959374bd 33 fields · synced May 30, 2026