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Pmi

FDA UDI

Class I (US FDA UDI)

by Progressive Medical, Inc.

Identity

Trade Name
PMI FDA UDI
Generic Name
Suturing unit, single-use FDA UDI
Device Name
PMI Disposable Bariatric Classic Closure Kit (3 piece) (1) PMI Disposable Bariatric Classic Closure Device, (1) PMI Disposable 10/12mm Suture Guide, (1) PMI Disposable 15mm 4-Hole Bariatric Suture Guide FDA UDI
Model / Reference
PMICCXLKT FDA UDI
Description
PMI Disposable Bariatric Classic Closure Kit (3 piece) (1) PMI Disposable Bariatric Classic Closure Device, (1) PMI Disposable 10/12mm Suture Guide, (1) PMI Disposable 15mm 4-Hole Bariatric Suture Guide FDA UDI

Identifiers

Primary DI / UDI-DI
00812608022342 FDA UDI
FDA Product Code
KDD FDA UDI
GMDN Term
Suturing unit, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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: Suturing unit, single-use

Pmi by Progressive Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suturing unit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 098d5ffa-de22-4815-9b15-e8735f76662b 33 fields · synced Jun 8, 2026