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Rtmed

FDA UDI

Class I (US FDA UDI)

by Shandong Haidike Medical Products Co., Ltd.

Identity

Trade Name
RTMED FDA UDI
Generic Name
Skin treatment/dressing-supportive limb/finger bandage, single-use FDA UDI
Model / Reference
Water proof type 70mm×19mm FDA UDI

Identifiers

Primary DI / UDI-DI
06971642800324 FDA UDI
FDA Product Code
NAC FDA UDI
GMDN Term
Skin treatment/dressing-supportive limb/finger bandage, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4018 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

FDA UDI

Category: Skin treatment/dressing-supportive limb/finger bandage, single-use

Rtmed by Shandong Haidike Medical Products Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin treatment/dressing-supportive limb/finger bandage, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Shandong Haidike Medical Products Co., Ltd.

Sources (1)

  • FDA UDI 1187f489-4f01-451e-b9e2-1e17953a688d 32 fields · synced May 30, 2026