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Alton

FDA UDI

Class I (US FDA UDI)

by Alton (Shanghai) Medical Instruments Co., Ltd.

Identity

Trade Name
Alton FDA UDI
Generic Name
Flexible endoscopic biopsy forceps, single-use FDA UDI
Model / Reference
AF-D2416BUC FDA UDI

Identifiers

Primary DI / UDI-DI
06970671381385 FDA UDI
FDA Product Code
FCL FDA UDI
GMDN Term
Flexible endoscopic biopsy forceps, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.1075 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

No

FDA UDI

Category: Flexible endoscopic biopsy forceps, single-use

Alton by Alton (Shanghai) Medical Instruments Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible endoscopic biopsy forceps, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4447d683-deaf-44ec-9821-fc7735aedf70 32 fields · synced May 30, 2026