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SpinMedix® Absorbable Fibrous Membrane

FDA UDI

Class II (US FDA UDI)

by Ningbo Guangyuan Zhixin Biological Technology Co., Ltd.

Identity

Trade Name
SpinMedix® Absorbable Fibrous Membrane FDA UDI
Generic Name
Extra-gynaecological surgical mesh, synthetic polymer, bioabsorbable FDA UDI
Model / Reference
ZK-010 FDA UDI

Identifiers

Primary DI / UDI-DI
06975222391097 FDA UDI
510(k) Number
K222220 FDA UDI
FDA Product Code
OWW FDA UDI
FTL FDA UDI
GMDN Term
Extra-gynaecological surgical mesh, synthetic polymer, bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.3300 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Extra-gynaecological surgical mesh, synthetic polymer, bioabsorbable

SpinMedix® Absorbable Fibrous Membrane by Ningbo Guangyuan Zhixin Biological Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Extra-gynaecological surgical mesh, synthetic polymer, bioabsorbable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0a7ee5cf-4a0c-4ab9-874f-197912f695f7 33 fields · synced May 30, 2026