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Lap-Band

FDA UDI

Class III (US FDA UDI)

by Apollo Endosurgery

Identity

Trade Name
LAP-BAND FDA UDI
Generic Name
Gastric band FDA UDI
Device Name
The LAP-BAND AP Adjustable Gastric Banding System with RapidPort EZ FDA UDI
Model / Reference
C-2365 FDA UDI
Description
The LAP-BAND AP Adjustable Gastric Banding System with RapidPort EZ FDA UDI

Identifiers

Catalog Number
C-2365 FDA UDI
Primary DI / UDI-DI
10811955020312 FDA UDI
FDA Product Code
LTI FDA UDI
GMDN Term
Gastric band FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Lap-Band by Apollo Endosurgery — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Apollo Endosurgery

Sources (1)

  • FDA UDI 1e611687-6ab3-429b-aa95-2352455f8594 36 fields · synced Jun 1, 2026