Apollo 2-0 Polypropylene Endobariatric Suture

FDA UDI

Class II (US FDA UDI)

by Apollo Endosurgery

Identity

Trade Name: Apollo 2-0 Polypropylene Endobariatric Suture FDA UDI
Generic Name: Suturing unit, single-use FDA UDI
Device Name: Apollo 2-0 Polypropylene Suture to be utilized with the Apollo ESG Dual and Single Channel Endobariatric suture system and the Apollo Revise Dual and Single Channel Endobariatric suture system FDA UDI
Model / Reference: PLY-G02-020-BAR FDA UDI
Description: Apollo 2-0 Polypropylene Suture to be utilized with the Apollo ESG Dual and Single Channel Endobariatric suture system and the Apollo Revise Dual and Single Channel Endobariatric suture system FDA UDI

Identifiers

Primary DI / UDI-DI: 00811955020827 FDA UDI
FDA Product Code: QTD FDA UDI
GMDN Term: Suturing unit, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 876.5983 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Conditional FDA UDI

Category: Suturing unit, single-use

Apollo 2-0 Polypropylene Endobariatric Suture by Apollo Endosurgery — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Apollo Endosurgery

Sources (1)

FDA UDI 927f5c23-1e9a-4013-acc2-a3fe39b5686c 34 fields · synced May 30, 2026