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Interseal®

FDA UDI

Class II (US FDA UDI)

by MicroPort Orthopedics Inc.

Identity

Trade Name
INTERSEAL® FDA UDI
Generic Name
Metallic acetabulum prosthesis FDA UDI
Device Name
APICAL HOLE PLUG W/ HEX HANDLE FDA UDI
Model / Reference
3818000200 FDA UDI
Description
APICAL HOLE PLUG W/ HEX HANDLE FDA UDI

Identifiers

Catalog Number
3818000200 FDA UDI
Primary DI / UDI-DI
M68438180002001 FDA UDI
FDA Product Code
LPH FDA UDI
GMDN Term
Metallic acetabulum prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3358 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

No

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

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Metallic acetabulum prosthesis

Interseal® by MicroPort Orthopedics Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metallic acetabulum prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 683c0aa1-63c3-424f-858a-5c13575c8c18 35 fields · synced Jun 9, 2026