← Back to catalogue

Magnum Medical

FDA UDI

Class I (US FDA UDI)

by Magnum Medical, Inc.

Identity

Trade Name
Magnum Medical FDA UDI
Generic Name
Medical tubing clip/clamp, temporary, non-calibrated, single-use FDA UDI
Device Name
U Clamp-Single Use FDA UDI
Model / Reference
05-2055 FDA UDI
Description
U Clamp-Single Use FDA UDI

Identifiers

Primary DI / UDI-DI
00810025360245 FDA UDI
FDA Product Code
KDC FDA UDI
GMDN Term
Medical tubing clip/clamp, temporary, non-calibrated, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Medical tubing clip/clamp, temporary, non-calibrated, single-use

Magnum Medical by Magnum Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical tubing clip/clamp, temporary, non-calibrated, 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

Manufacturer
Magnum Medical, Inc.

Sources (1)

  • FDA UDI 1f968aef-cb65-4658-9444-6cb78dff2fc0 33 fields · synced May 29, 2026