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rescuCLAMP™ Catheter Repair Clamp

FDA UDI

Class I (US FDA UDI)

by Cardio Med Supplies, Inc.

Identity

Trade Name
rescuCLAMP™ Catheter Repair Clamp FDA UDI
Generic Name
Medical tubing clip/clamp, temporary, non-calibrated, single-use FDA UDI
Device Name
The Catheter Repair Clamp is designed with additional openings along the side and the top of the clamp to be quickly added or removed from tubing. FDA UDI
Model / Reference
1.5 FDA UDI
Description
The Catheter Repair Clamp is designed with additional openings along the side and the top of the clamp to be quickly added or removed from tubing. FDA UDI

Identifiers

Catalog Number
CM-604 FDA UDI
Primary DI / UDI-DI
36641670011528 FDA UDI
FDA Product Code
FKK FDA UDI
GMDN Term
Medical tubing clip/clamp, temporary, non-calibrated, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.4730 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

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

rescuCLAMP™ Catheter Repair Clamp by Cardio Med Supplies, 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

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Manufacturer

Manufacturer
Cardio Med Supplies, Inc.

Sources (1)

  • FDA UDI 0677ff50-29f4-4e8f-ba56-a0309990794b 34 fields · synced May 30, 2026