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Ultraclamp

FDA UDI

Class I (US FDA UDI)

by Baxter Healthcare Corp

Identity

Trade Name
ULTRACLAMP FDA UDI
Generic Name
Medical tubing clip/clamp, temporary, non-calibrated, reusable FDA UDI
Device Name
UltraClamp Tubing is designed to facilitate clamping of tubing on the UltraBag Container or any Baxter Y-Set. The clamp is specifically designed to assist individuals who experience difficulty in operating other ancillary clamps or pre-attached clamps. FDA UDI
Model / Reference
5C4957 FDA UDI
Description
UltraClamp Tubing is designed to facilitate clamping of tubing on the UltraBag Container or any Baxter Y-Set. The clamp is specifically designed to assist individuals who experience difficulty in operating other ancillary clamps or pre-attached clamps. FDA UDI

Identifiers

Catalog Number
5C4957 FDA UDI
Primary DI / UDI-DI
00085412070643 FDA UDI
FDA Product Code
FKK FDA UDI
GMDN Term
Medical tubing clip/clamp, temporary, non-calibrated, reusable 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

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

Ultraclamp by Baxter Healthcare Corp — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI df6df18f-789a-4b3a-8ea4-0303164e5c78 36 fields · synced May 30, 2026