Rapid Seal Tube Sealer SE470

FDA UDIEUDAMED

Class I (US FDA UDI)

by Centron Corporation

Identity

Trade Name: Rapid Seal Tube Sealer SE470 FDA UDI
Generic Name: Blood donor bag tube divider/sealer FDA UDI
Device Name: The Rapid Seal SE470 is a compact and lightweight tube sealer with a hand unit. The device is specially designed to seal the cord blood freezing bags and tubing. Long and slim sealing head is suitable for sealing the channels between two compartments of bag. FDA UDI
Model / Reference: SE470 FDA UDI
Description: The Rapid Seal SE470 is a compact and lightweight tube sealer with a hand unit. The device is specially designed to seal the cord blood freezing bags and tubing. Long and slim sealing head is suitable for sealing the channels between two compartments of bag. FDA UDI

Identifiers

Catalog Number: SE470 FDA UDI
Primary DI / UDI-DI: 08809241442233 FDA UDI
FDA Product Code: KSD FDA UDI
GMDN Term: Blood donor bag tube divider/sealer FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 864.9750 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size: Width — 10.6 Centimeter FDA UDI
Height — 15.0 Centimeter FDA UDI
Depth — 26.0 Centimeter FDA UDI
Weight — 3.5 Kilogram FDA UDI

Category: Blood donor bag tube divider/sealer

Rapid Seal Tube Sealer SE470 by Centron Corporation — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

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Rapid Seal Tube Sealer SE340 — CENTRON CORPORATION · Class I
Rapid Seal Tube Sealer SE530 — CENTRON CORPORATION · Class I

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
EUDAMED	European Union	MDR	—	Class I	Unknown
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Centron Corporation

Sources (2)

FDA UDI 8e252f93-2fd4-4f46-870e-018e962e790f 36 fields · synced Jun 20, 2026
EUDAMED 1 fields · synced Jun 1, 2026