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H. Lee SafeSheath® Sealing Adapter

FDA UDI

Class II (US FDA UDI)

by Merit Medical Systems, Inc.

Identity

Trade Name
H. Lee SafeSheath® Sealing Adapter FDA UDI
Generic Name
Haemostasis valve FDA UDI
Model / Reference
00884450505366 FDA UDI

Identifiers

Catalog Number
SS-SA-09 FDA UDI
Primary DI / UDI-DI
00884450505366 FDA UDI
FDA Product Code
DTL FDA UDI
GMDN Term
Haemostasis valve FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4290 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Category: Haemostasis valve

H. Lee SafeSheath® Sealing Adapter by Merit Medical Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Haemostasis valve.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 165287f2-2b9f-432c-835a-2ec96ac8cf2c 34 fields · synced Jun 9, 2026