← Back to catalogue

Celt ACD Vascular Closure Device 6F_ESP

FDA UDI

Class III (US FDA UDI)

by Vasorum, Ltd.

Identity

Trade Name
Celt ACD Vascular Closure Device 6F_ESP FDA UDI
Generic Name
Implantable vascular closure clip FDA UDI
Device Name
Celt ACD Vascular Closure Device 6F_ESP FDA UDI
Model / Reference
KCLT-06 FDA UDI
Description
Celt ACD Vascular Closure Device 6F_ESP FDA UDI

Identifiers

Primary DI / UDI-DI
05391530280099 FDA UDI
PMA Number
P150006 FDA UDI
FDA Product Code
MGB FDA UDI
GMDN Term
Implantable vascular closure clip FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Catheter Gauge — 6 French FDA UDI

Category: Implantable vascular closure clip

Celt ACD Vascular Closure Device 6F_ESP by Vasorum, Ltd. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Implantable vascular closure clip.

Cleared under the same submission

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
Vasorum, Ltd.

Sources (1)

  • FDA UDI 51de286e-8ab7-44d6-b50b-108c2494644e 36 fields · synced Jun 1, 2026