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Saeed

FDA UDI

Class II (US FDA UDI)

by Cook Incorporated

Identity

Trade Name
Saeed FDA UDI
Generic Name
Oesophageal endoscopic ligator, single-use FDA UDI
Device Name
Six Shooter Saeed Multi-Band Ligator FDA UDI
Model / Reference
G25121 FDA UDI
Description
Six Shooter Saeed Multi-Band Ligator FDA UDI

Identifiers

Catalog Number
MBL-6-XL-I FDA UDI
Primary DI / UDI-DI
00827002251212 FDA UDI
FDA Product Code
MND FDA UDI
GMDN Term
Oesophageal endoscopic ligator, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.4400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

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

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: Oesophageal endoscopic ligator, single-use

Saeed by Cook Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Oesophageal endoscopic ligator, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cook Incorporated

Sources (1)

  • FDA UDI 282673e6-0b87-420d-bec8-05039fd659d3 36 fields · synced Jun 8, 2026