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Tiannuo / Tnmed

FDA UDI

Class I (US FDA UDI)

by Lianyungang Tiannuo Optical Instrument Co., Ltd.

Identity

Trade Name
TIANNUO / TNMED FDA UDI
Generic Name
Manually-adjusted lensmeter, line-powered FDA UDI
Model / Reference
TN-28MX FDA UDI

Identifiers

Primary DI / UDI-DI
06945033901983 FDA UDI
FDA Product Code
HLM FDA UDI
GMDN Term
Manually-adjusted lensmeter, line-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.1425 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Manually-adjusted lensmeter, line-powered

Tiannuo / Tnmed by Lianyungang Tiannuo Optical Instrument Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manually-adjusted lensmeter, line-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9fcc6ad3-cb3b-46b3-a53e-1256f2ee8b43 32 fields · synced May 30, 2026