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4WEB Medical

FDA UDI

Class II (US FDA UDI)

by 4Web Medical, Inc.

Identity

Trade Name
4WEB Medical FDA UDI
Generic Name
Metallic osteotomy fusion cage, non-customized FDA UDI
Model / Reference
ATS-3535300 FDA UDI

Identifiers

Catalog Number
ATS-3535300 FDA UDI
Primary DI / UDI-DI
00810074756341 FDA UDI
FDA Product Code
SAI FDA UDI
GMDN Term
Metallic osteotomy fusion cage, non-customized FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Metallic osteotomy fusion cage, non-customized

4WEB Medical by 4Web Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metallic osteotomy fusion cage, non-customized.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
4Web Medical, Inc.

Sources (1)

  • FDA UDI 219e03b6-294e-4535-8f88-b0d100b27507 33 fields · synced May 30, 2026