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Contodo Medicsl Supplies

FDA UDI

Class II (US FDA UDI)

by Contodo LLC

Identity

Trade Name
Contodo Medicsl Supplies FDA UDI
Generic Name
Surgical/examination garment kit FDA UDI
Model / Reference
CTMS0007 FDA UDI

Identifiers

Primary DI / UDI-DI
00860013348786 FDA UDI
510(k) Number
K212718 FDA UDI
FDA Product Code
FYA FDA UDI
GMDN Term
Surgical/examination garment kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4040 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

No

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
Ethylene Oxide FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Surgical/examination garment kit

Contodo Medicsl Supplies by Contodo LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical/examination garment kit.

Cleared under the same submission

K212718 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Contodo LLC

Sources (1)

  • FDA UDI dda8298e-ef97-4bea-8419-2bc7207fe6a9 33 fields · synced May 30, 2026