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Mani Sutures Nylon - 7-0 Nylon

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref 38

by Mani, Inc.

Identity

Trade Name
MANI SUTURES NYLON - 7-0 NYLON EUDAMED
MANI Sutures Nylon FDA UDI
Generic Name
Nylon suture, non-bioabsorbable, monofilament FDA UDI
Device Name
MANI SUTURES NYLON EUDAMED
Model / Reference
38 EUDAMEDFDA UDI

Identifiers

Catalog Number
38 FDA UDI
Primary DI / UDI-DI
04546951500313 EUDAMEDFDA UDI
Basic UDI-DI
B-04546951500313 EUDAMED
FDA Product Code
GAR FDA UDI
EMDN Code
H010201010101 POLYAMIDE MONOFILAMENT WITH NEEDLE EUDAMED
GMDN Term
Nylon suture, non-bioabsorbable, monofilament FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
878.5020 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Mani Sutures Nylon - 7-0 Nylon by Mani, Inc. — Class IIb — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mani, Inc.
EUDAMED SRN
JP-MF-000017860
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (2)

  • EUDAMED ee501aff-a274-4e69-9586-8a2555eed273 61 fields · synced Jun 18, 2026
  • FDA UDI 66a91739-8675-496a-b4cc-4239368c1367 33 fields · synced May 30, 2026