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Ancora

FDA UDI

Class II (US FDA UDI)

by Aspero Medical, Inc.

Identity

Trade Name
Ancora FDA UDI
Generic Name
Endoscopic overtube, single-use FDA UDI
Device Name
Balloon Overtube Assembly, package of 4 FDA UDI
Model / Reference
Ancora-SB 4-pack FDA UDI
Description
Balloon Overtube Assembly, package of 4 FDA UDI

Identifiers

Primary DI / UDI-DI
10860006600805 FDA UDI
510(k) Number
K231323 FDA UDI
FDA Product Code
FDA FDA UDI
FED FDA UDI
GMDN Term
Endoscopic overtube, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

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

Category: Endoscopic overtube, single-use

Ancora by Aspero Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic overtube, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f06e459f-6e18-491f-b782-f6a708ef6c65 34 fields · synced May 30, 2026