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Biotem

FDA UDI

Class I (US FDA UDI)

by Biotem Co., ltd

Identity

Trade Name
Biotem FDA UDI
Generic Name
Dental implant system FDA UDI
Device Name
Biotem AR SOLID LAB ANALOG 4.5mm Ⅹ 7.0mm(length) FDA UDI
Model / Reference
LAAS4507 FDA UDI
Description
Biotem AR SOLID LAB ANALOG 4.5mm Ⅹ 7.0mm(length) FDA UDI

Identifiers

Primary DI / UDI-DI
08800036212796 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implant system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 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

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Category: Dental implant system

Biotem by Biotem Co., ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biotem Co., ltd

Sources (1)

  • FDA UDI be503b08-199e-4368-ac87-a02b2688173a 33 fields · synced May 31, 2026